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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Detalhes bibliográficos
Publicado no:FEBS Open Bio
Main Authors: Li, Chengcheng, Vargas‐Franco, Dorianmarie, Saha, Madhurima, Davis, Rachel M., Manko, Kelsey A., Draper, Isabelle, Pacak, Christina A., Kang, Peter B.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2020
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7780119/
https://ncbi.nlm.nih.gov/pubmed/33159715
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/2211-5463.13031
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