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...

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Bibliografiske detaljer
Main Authors: Pedrola, Laia, Espert, Antonio, Valdés-Sánchez, Teresa, Sánchez-Piris, Maribel, Sirkowski, Erich E, Scherer, Steven S, Fariñas, Isabel, Palau, Francesc
Format: Artigo
Sprog:Inglês
Udgivet: Blackwell Publishing Ltd 2008
Fag:
Images in Cellular / Molecular Medicine
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2570022/
https://ncbi.nlm.nih.gov/pubmed/18021315
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1582-4934.2007.00158.x
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