Cargando…

Cell expression of GDAP1 in the nervous system and pathogenesis of Charcot-Marie-Tooth type 4A disease

Mutations in the mitochondrial protein GDAP1 are the cause of Charcot-Marie-Tooth type 4A disease (CMT4A), a severe form of peripheral neuropathy associated with either demyelinating, axonal or intermediate pheno-types. GDAP1 is located in the outer mitochondrial membrane and it seems that may be re...

Descripción completa

Detalles Bibliográficos
Autores principales: Pedrola, Laia, Espert, Antonio, Valdés-Sánchez, Teresa, Sánchez-Piris, Maribel, Sirkowski, Erich E, Scherer, Steven S, Fariñas, Isabel, Palau, Francesc
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2570022/
https://www.ncbi.nlm.nih.gov/pubmed/18021315
http://dx.doi.org/10.1111/j.1582-4934.2007.00158.x