Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy
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19p13.2 Google OMIM PubMed [Charcot-Marie-Tooth disease] Charcot-Marie-Tooth disease, dominant intermediate B *Gene map locus 19p13.2 CMTDI1 CMTDIB Charcot-Marie-Tooth neuropathy, dominant intermediate B DI-CMTB [Clinical features: Charcot-Marie-Tooth phenotype; neutropenia; cataracts] [Inheritance: autosomal dominant] |
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Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy |
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy |
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Edited by Aldo Campana,
August 21, 2012
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