Matches in Nanopublications for { ?s ?p "[More recently, progranulin gene mutations were recognized in association with the familial form of FTLD and a hexanucleotide repetition in C9ORF72 has been shown to be responsible for familial FTLD and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP353018.RA4R9lmxi4Fgvh9t9co75fQm4RaQafM4la6-CYOINGGJA130_assertion description "[More recently, progranulin gene mutations were recognized in association with the familial form of FTLD and a hexanucleotide repetition in C9ORF72 has been shown to be responsible for familial FTLD and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP353018.RA4R9lmxi4Fgvh9t9co75fQm4RaQafM4la6-CYOINGGJA130_provenance.
- NP413217.RAnftOzI8zg8TVGOp_CKOFth5_1pswtijJkE9LrJeQSKA130_assertion description "[More recently, progranulin gene mutations were recognized in association with the familial form of FTLD and a hexanucleotide repetition in C9ORF72 has been shown to be responsible for familial FTLD and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP413217.RAnftOzI8zg8TVGOp_CKOFth5_1pswtijJkE9LrJeQSKA130_provenance.
- assertion description "[More recently, progranulin gene mutations were recognized in association with the familial form of FTLD and a hexanucleotide repetition in C9ORF72 has been shown to be responsible for familial FTLD and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[More recently, progranulin gene mutations were recognized in association with the familial form of FTLD and a hexanucleotide repetition in C9ORF72 has been shown to be responsible for familial FTLD and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP977326.RAXKbpZG6JMOVkS0F02rSTBBqPLnfPqE242YuwuQiTyqs130_assertion description "[More recently, progranulin gene mutations were recognized in association with the familial form of FTLD and a hexanucleotide repetition in C9ORF72 has been shown to be responsible for familial FTLD and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977326.RAXKbpZG6JMOVkS0F02rSTBBqPLnfPqE242YuwuQiTyqs130_provenance.
- assertion description "[More recently, progranulin gene mutations were recognized in association with the familial form of FTLD and a hexanucleotide repetition in C9ORF72 has been shown to be responsible for familial FTLD and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[More recently, progranulin gene mutations were recognized in association with the familial form of FTLD and a hexanucleotide repetition in C9ORF72 has been shown to be responsible for familial FTLD and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP977323.RApMF48-V_puqARScQ9_WDG4dAi-r1Xf2PYHJqVnF5VRY130_assertion description "[More recently, progranulin gene mutations were recognized in association with the familial form of FTLD and a hexanucleotide repetition in C9ORF72 has been shown to be responsible for familial FTLD and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977323.RApMF48-V_puqARScQ9_WDG4dAi-r1Xf2PYHJqVnF5VRY130_provenance.
- NP977325.RAp9KSVEMIquq1jg_T6WvhO2fqGPiqYT7SekrhWUhCZoI130_assertion description "[More recently, progranulin gene mutations were recognized in association with the familial form of FTLD and a hexanucleotide repetition in C9ORF72 has been shown to be responsible for familial FTLD and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977325.RAp9KSVEMIquq1jg_T6WvhO2fqGPiqYT7SekrhWUhCZoI130_provenance.
- NP433938.RA8aEa2HHCFAX11uu-Va339hNg05Gf2A_6_qcTNkRw_Gk130_assertion description "[More recently, progranulin gene mutations were recognized in association with the familial form of FTLD and a hexanucleotide repetition in C9ORF72 has been shown to be responsible for familial FTLD and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP433938.RA8aEa2HHCFAX11uu-Va339hNg05Gf2A_6_qcTNkRw_Gk130_provenance.
- NP977324.RA4T3o4-PC95wXD0rLr9Qz91XY-Ki1OWv1oPRZVpQlU2E130_assertion description "[More recently, progranulin gene mutations were recognized in association with the familial form of FTLD and a hexanucleotide repetition in C9ORF72 has been shown to be responsible for familial FTLD and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977324.RA4T3o4-PC95wXD0rLr9Qz91XY-Ki1OWv1oPRZVpQlU2E130_provenance.