EDMD-Causing Emerin Mutant Myogenic Progenitors Exhibit Impaired Differentiation Using Similar Mechanisms

Mutations in the gene encoding emerin (EMD) cause Emery–Dreifuss muscular dystrophy (EDMD1), an inherited disorder characterized by progressive skeletal muscle wasting, irregular heart rhythms and contractures of major tendons. The skeletal muscle defects seen in EDMD are caused by failure of muscle...

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Detalles Bibliográficos
Autores principales: Iyer, Ashvin, Holaska, James M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349064/
https://www.ncbi.nlm.nih.gov/pubmed/32549231
http://dx.doi.org/10.3390/cells9061463

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349064/
https://www.ncbi.nlm.nih.gov/pubmed/32549231
http://dx.doi.org/10.3390/cells9061463

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