Matches in Nanopublications for { ?s ?p "[Mutations in the myotubularin (MTM)-related protein 2 (MTMR2) gene are responsible for the severe autosomal recessive neuropathy Charcot-Marie-Tooth disease type 4B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP675790.RADqJvQ_XL8a-xijT5jFNBgDzQ-NmkxbnMjyCr-blxRQA130_assertion description "[Mutations in the myotubularin (MTM)-related protein 2 (MTMR2) gene are responsible for the severe autosomal recessive neuropathy Charcot-Marie-Tooth disease type 4B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675790.RADqJvQ_XL8a-xijT5jFNBgDzQ-NmkxbnMjyCr-blxRQA130_provenance.
- NP637641.RAmBaoKT86iMNJVsit76xgSRvmkuuUvHaCt5UftZw6Ja8130_assertion description "[Mutations in the myotubularin (MTM)-related protein 2 (MTMR2) gene are responsible for the severe autosomal recessive neuropathy Charcot-Marie-Tooth disease type 4B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP637641.RAmBaoKT86iMNJVsit76xgSRvmkuuUvHaCt5UftZw6Ja8130_provenance.
- NP716991.RA5cicFnWWApnZjxdEaoYeB1GObZ8saHO9oF-DFCtu2Rk130_assertion description "[Mutations in the myotubularin (MTM)-related protein 2 (MTMR2) gene are responsible for the severe autosomal recessive neuropathy Charcot-Marie-Tooth disease type 4B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP716991.RA5cicFnWWApnZjxdEaoYeB1GObZ8saHO9oF-DFCtu2Rk130_provenance.
- NP810705.RARyLNLoHEwBd9FOKg91mjH8pXrC9GeqRVgTTkDrdVDlw130_assertion description "[Mutations in the myotubularin (MTM)-related protein 2 (MTMR2) gene are responsible for the severe autosomal recessive neuropathy Charcot-Marie-Tooth disease type 4B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810705.RARyLNLoHEwBd9FOKg91mjH8pXrC9GeqRVgTTkDrdVDlw130_provenance.
- assertion description "[Mutations in the myotubularin (MTM)-related protein 2 (MTMR2) gene are responsible for the severe autosomal recessive neuropathy Charcot-Marie-Tooth disease type 4B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the myotubularin (MTM)-related protein 2 (MTMR2) gene are responsible for the severe autosomal recessive neuropathy Charcot-Marie-Tooth disease type 4B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP415969.RAXtrjIwlyPEgRLx2suRDLejWmNe-8HUVR4p9yT-UOc8c130_assertion description "[Mutations in the myotubularin (MTM)-related protein 2 (MTMR2) gene are responsible for the severe autosomal recessive neuropathy Charcot-Marie-Tooth disease type 4B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP415969.RAXtrjIwlyPEgRLx2suRDLejWmNe-8HUVR4p9yT-UOc8c130_provenance.
- NP855938.RAOZk57gpU54jyaTP88gBrQAbxKxolqFk8GzWltlLH_ow130_assertion description "[Mutations in the myotubularin (MTM)-related protein 2 (MTMR2) gene are responsible for the severe autosomal recessive neuropathy Charcot-Marie-Tooth disease type 4B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP855938.RAOZk57gpU54jyaTP88gBrQAbxKxolqFk8GzWltlLH_ow130_provenance.
- NP810715.RAzqX-lhhOew-M6LdPg7zW6lr83qvH_Vo2dwmXfcpucSY130_assertion description "[Mutations in the myotubularin (MTM)-related protein 2 (MTMR2) gene are responsible for the severe autosomal recessive neuropathy Charcot-Marie-Tooth disease type 4B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810715.RAzqX-lhhOew-M6LdPg7zW6lr83qvH_Vo2dwmXfcpucSY130_provenance.
- NP415968.RAEiwf3bfDRORKcNzaqByRmwygvPghIZ6YIqamVjpOpb4130_assertion description "[Mutations in the myotubularin (MTM)-related protein 2 (MTMR2) gene are responsible for the severe autosomal recessive neuropathy Charcot-Marie-Tooth disease type 4B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP415968.RAEiwf3bfDRORKcNzaqByRmwygvPghIZ6YIqamVjpOpb4130_provenance.