Myelin protein zero gene mutated in Charcot-Marie-tooth type 1B patients.

Autosomal dominant of Charcot-Marie-Tooth disease (CMT), whose gene is type 1B (CMT1B), has slow nerve conduction with demyelinated Schwann cells. In this study the abundant peripheral myelin protein zero (MPZ) gene, MPZ, was mapped 130 kb centromeric to the Fc receptor immunoglobulin gene cluster i...

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Detalhes bibliográficos
Main Authors: Su, Y, Brooks, D G, Li, L, Lepercq, J, Trofatter, J A, Ravetch, J V, Lebo, R V
Formato: Artigo
Idioma:Inglês
Publicado em: 1993
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC47877/
https://ncbi.nlm.nih.gov/pubmed/7504284
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