Energy metabolism and mitochondrial defects in X-linked Charcot-Marie-Tooth (CMTX6) iPSC-derived motor neurons with the p.R158H PDK3 mutation

Charcot-Marie-Tooth (CMT) is a group of inherited diseases clinically and genetically heterogenous, characterised by length dependent degeneration of axons of the peripheral nervous system. A missense mutation (p.R158H) in the pyruvate dehydrogenase kinase 3 gene (PDK3) has been identified as the ge...

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Detalles Bibliográficos
Autores principales: Perez-Siles, G., Cutrupi, A., Ellis, M., Screnci, R., Mao, D., Uesugi, M., Yiu, Eppie M., Ryan, Monique M., Choi, B. O., Nicholson, G., Kennerson, M. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275085/
https://www.ncbi.nlm.nih.gov/pubmed/32504000
http://dx.doi.org/10.1038/s41598-020-66266-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275085/
https://www.ncbi.nlm.nih.gov/pubmed/32504000
http://dx.doi.org/10.1038/s41598-020-66266-5

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