Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP409221.RAYMC3EpOy8lM1Af0ndc8ySYbiDcE2tWmDX5ZqC4KMKYA130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409221.RAYMC3EpOy8lM1Af0ndc8ySYbiDcE2tWmDX5ZqC4KMKYA130_provenance.
• NP412817.RAdhPTJsQ1FTFjj_61nRJkYDKQeXcC-PYEd-zXK63I_bM130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412817.RAdhPTJsQ1FTFjj_61nRJkYDKQeXcC-PYEd-zXK63I_bM130_provenance.
• NP1334247.RAbpYrca04Sa8FuoDyrgdYBiaJyNn_NmArJ2Vg7ebezh4130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334247.RAbpYrca04Sa8FuoDyrgdYBiaJyNn_NmArJ2Vg7ebezh4130_provenance.
• NP1334251.RAcJcKoC9i03WUYvQtgqU1NLGwL9aszCZos2cnrfQ8H80130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334251.RAcJcKoC9i03WUYvQtgqU1NLGwL9aszCZos2cnrfQ8H80130_provenance.
• NP409241.RACNKIryTZqM01ouGyql6nMFuGN1xoEymzRKbu1y_UZQA130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409241.RACNKIryTZqM01ouGyql6nMFuGN1xoEymzRKbu1y_UZQA130_provenance.
• NP1334243.RAA01S59Io10xHu4DdrvM33nonC59ylFP8LoM508q8leE130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334243.RAA01S59Io10xHu4DdrvM33nonC59ylFP8LoM508q8leE130_provenance.
• NP1334242.RAgbAbQEpEvdDNmnQPr81QzLtpT_6XI9AA-VJ_3VAvKIk130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334242.RAgbAbQEpEvdDNmnQPr81QzLtpT_6XI9AA-VJ_3VAvKIk130_provenance.
• NP1334245.RAmZH9tIz4kZB5EYi12JjFruXjQpAA2LhsIkWEXA9y1NM130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334245.RAmZH9tIz4kZB5EYi12JjFruXjQpAA2LhsIkWEXA9y1NM130_provenance.
• NP1334246.RAlicoqMvklbj1dlngtfImOPAW8ah2JrPh6JJwoX5RGms130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334246.RAlicoqMvklbj1dlngtfImOPAW8ah2JrPh6JJwoX5RGms130_provenance.
• NP1334249.RAkxHNFILaXHnS9Lwu-hfDfF8VilxglQOrvo_zB92ryu4130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334249.RAkxHNFILaXHnS9Lwu-hfDfF8VilxglQOrvo_zB92ryu4130_provenance.
• NP1334253.RArzkI2hE9VHH8cJ2OHmq7Nr6eRkvhRijeEoqu9Gjbfjc130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334253.RArzkI2hE9VHH8cJ2OHmq7Nr6eRkvhRijeEoqu9Gjbfjc130_provenance.
• NP1334255.RAs_RPM4B6ugu7yZIH3_6_UK-gMDX3iTtpHhmyo3TLIkk130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334255.RAs_RPM4B6ugu7yZIH3_6_UK-gMDX3iTtpHhmyo3TLIkk130_provenance.
• NP409205.RA7GnkgYlQWR8bKcM4ztG2YSy6_LlaM-2RC7h64YftnRc130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409205.RA7GnkgYlQWR8bKcM4ztG2YSy6_LlaM-2RC7h64YftnRc130_provenance.
• NP409242.RA3Javw02wzfOm3tQ2Rh_cMC_bPHGOC5c87XGzhNI0c54130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409242.RA3Javw02wzfOm3tQ2Rh_cMC_bPHGOC5c87XGzhNI0c54130_provenance.
• NP412833.RA9Dtq-E6WVHoTrLToAfYI5E2WYM_35DJ0Za0J49UDA5w130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412833.RA9Dtq-E6WVHoTrLToAfYI5E2WYM_35DJ0Za0J49UDA5w130_provenance.
• NP412853.RA_oeBPRtRZb-A6tp7NSGeP_4IWMOB-0WOk690hXblGMw130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412853.RA_oeBPRtRZb-A6tp7NSGeP_4IWMOB-0WOk690hXblGMw130_provenance.
• NP412874.RA09Ud5Qe9S-BdwVQK9ay3i9iUvE03gBTmfPZV1JcLsMA130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412874.RA09Ud5Qe9S-BdwVQK9ay3i9iUvE03gBTmfPZV1JcLsMA130_provenance.
• NP412681.RAGcb5HibjYGQP7m1swflRXeyQM6pfgGh4i9kNtUBQfAM130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412681.RAGcb5HibjYGQP7m1swflRXeyQM6pfgGh4i9kNtUBQfAM130_provenance.
• NP412852.RAIZ7MA_CDVy0MbjWeggQEKumqWdTWanAOBdfBAOov_1k130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412852.RAIZ7MA_CDVy0MbjWeggQEKumqWdTWanAOBdfBAOov_1k130_provenance.
• NP409035.RAHpI6gGJNjcv7jg0cJ9E09LkTyWwwjPbrk2jy_8ai8nA130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409035.RAHpI6gGJNjcv7jg0cJ9E09LkTyWwwjPbrk2jy_8ai8nA130_provenance.
• NP409265.RAJqePO3h_rEToGZisKndI-XOaIJryeCrWBJWX53K2Wu8130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409265.RAJqePO3h_rEToGZisKndI-XOaIJryeCrWBJWX53K2Wu8130_provenance.
• NP1334241.RAO-G_8u_G0hvW58NUojitEWMdH62ejo47tgPKDTEO0hs130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334241.RAO-G_8u_G0hvW58NUojitEWMdH62ejo47tgPKDTEO0hs130_provenance.
• NP1334244.RAGsCIzC8DHALZPUv2KYt6pH6_c_cnlpatpYAnFCamm4k130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334244.RAGsCIzC8DHALZPUv2KYt6pH6_c_cnlpatpYAnFCamm4k130_provenance.
• NP1334248.RAKwpANhbCdXYH9XJxDShhArvkOqa2tKQHPr6b_nG1t2Q130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334248.RAKwpANhbCdXYH9XJxDShhArvkOqa2tKQHPr6b_nG1t2Q130_provenance.
• NP1334250.RAPflVkA5_sLfMojHRMXC60t7JoFt4s863PwiIB5XNp08130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334250.RAPflVkA5_sLfMojHRMXC60t7JoFt4s863PwiIB5XNp08130_provenance.
• NP1334256.RAEk2rjVi3AItl6j1EM0d1x0nB1UHYAfNF-sEv39HIg7g130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334256.RAEk2rjVi3AItl6j1EM0d1x0nB1UHYAfNF-sEv39HIg7g130_provenance.
• NP1334252.RA0c5YOvpP7aAWLy0B2yYlao8axfKFzQbBKzGrekFbLZU130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334252.RA0c5YOvpP7aAWLy0B2yYlao8axfKFzQbBKzGrekFbLZU130_provenance.
• NP1334254.RAxabCrzWycaikb_ivsR081WVrvT1Cf9Uc0pjvy0Yq75A130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334254.RAxabCrzWycaikb_ivsR081WVrvT1Cf9Uc0pjvy0Yq75A130_provenance.