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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Bibliografski detalji
Izdano u:FEBS Open Bio
Glavni autori: Li, Chengcheng, Vargas‐Franco, Dorianmarie, Saha, Madhurima, Davis, Rachel M., Manko, Kelsey A., Draper, Isabelle, Pacak, Christina A., Kang, Peter B.
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2020
Teme:
Research Articles
Online pristup: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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