A carregar...

Charcot-Marie-Tooth neuropathy type 2A: novel mutations in the mitofusin 2 gene (MFN2)

BACKGROUND: Charcot-Marie-Tooth neuropathies are a group of genetically heterogeneous diseases of the peripheral nervous system. Mutations in the MFN2 gene have been reported as the primary cause of Charcot-Marie-Tooth disease type 2A. METHODS: Patients with the clinical diagnosis of Charcot-Marie-T...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Engelfried, Kathrin, Vorgerd, Matthias, Hagedorn, Michaela, Haas, Gerhard, Gilles, Jürgen, Epplen, Jörg T, Meins, Moritz
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2006
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1524942/
https://ncbi.nlm.nih.gov/pubmed/16762064
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-7-53
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!