Megf10 deficiency impairs skeletal muscle stem cell migration and muscle regeneration

Biallelic loss‐of‐function MEGF10 mutations lead to MEGF10 myopathy, also known as early onset myopathy with areflexia, respiratory distress, and dysphagia (EMARDD). MEGF10 is expressed in muscle satellite cells, but the contribution of satellite cell dysfunction to MEGF10 myopathy is unclear. Myofi...

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Detalles Bibliográficos
Autores principales: Li, Chengcheng, Vargas‐Franco, Dorianmarie, Saha, Madhurima, Davis, Rachel M., Manko, Kelsey A., Draper, Isabelle, Pacak, Christina A., Kang, Peter B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7780119/
https://www.ncbi.nlm.nih.gov/pubmed/33159715
http://dx.doi.org/10.1002/2211-5463.13031

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7780119/
https://www.ncbi.nlm.nih.gov/pubmed/33159715
http://dx.doi.org/10.1002/2211-5463.13031

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