A Second Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 19q13.3

Autosomal recessive Charcot-Marie-Tooth disease (CMT) represents a heterogeneous group of disorders affecting the peripheral nervous system. The axonal form of the disease is designated as ”CMT type 2” (CMT2), and one locus (1q21.2-q21.3) has been reported for the autosomal recessive form. Here we r...

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Detalhes bibliográficos
Main Authors: Leal, Alejandro, Morera, Bernal, Del Valle, Gerardo, Heuss, Dieter, Kayser, Corinna, Berghoff, Martin, Villegas, Ramón, Hernández, Erick, Méndez, María, Hennies, Hans Christian, Neundörfer, Bernhard, Barrantes, Ramiro, Reis, André, Rautenstrauss, Bernd
Formato: Artigo
Idioma:Inglês
Publicado em: The American Society of Human Genetics 2001
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1234926/
https://ncbi.nlm.nih.gov/pubmed/11112660
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