Altered in vitro muscle differentiation in X-linked myopathy with excessive autophagy

X-linked myopathy with excessive autophagy (XMEA) is a genetic disease associated with weakness of the proximal muscles. It is caused by mutations in the VMA21 gene, coding for a chaperone that functions in the vacuolar ATPase (v-ATPase) assembly. Mutations associated with lower content of assembled...

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Detalles Bibliográficos
Autores principales: Fernandes, Stephanie A., Almeida, Camila F., Souza, Lucas S., Lazar, Monize, Onofre-Oliveira, Paula, Yamamoto, Guilherme L., Nogueira, Letícia, Tasaki, Letícia Y., Cardoso, Rafaela R., Pavanello, Rita C. M., Silva, Helga C. A., Ferrari, Merari F. R., Bigot, Anne, Mouly, Vincent, Vainzof, Mariz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994946/
https://www.ncbi.nlm.nih.gov/pubmed/31826868
http://dx.doi.org/10.1242/dmm.041244

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994946/
https://www.ncbi.nlm.nih.gov/pubmed/31826868
http://dx.doi.org/10.1242/dmm.041244

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