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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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Detalles Bibliográficos
Autores principales: Schiavon, Cara R., Shadel, Gerald S., Manor, Uri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7882694/
https://www.ncbi.nlm.nih.gov/pubmed/33598463
http://dx.doi.org/10.3389/fcell.2021.624823