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Impaired Mitochondrial Mobility in Charcot-Marie-Tooth Disease

Charcot-Marie-Tooth (CMT) disease is a progressive, peripheral neuropathy and the most commonly inherited neurological disorder. Clinical manifestations of CMT mutations are typically limited to peripheral neurons, the longest cells in the body. Currently, mutations in at least 80 different genes ar...

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Detalhes bibliográficos
Publicado no:Front Cell Dev Biol
Main Authors: Schiavon, Cara R., Shadel, Gerald S., Manor, Uri
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7882694/
https://ncbi.nlm.nih.gov/pubmed/33598463
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcell.2021.624823
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