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Myopathy-causing Actin Mutations Promote Defects in Serum Response Factor Signaling
Mutations in the gene encoding alpha skeletal muscle actin (ACTA1) account for around 20% of patients with the muscular disorder nemaline myopathy. Nemaline myopathy is a muscular wasting disease similar to muscular dystrophy, but distinguished by deposits of actin and actin-associated proteins near...
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| Principais autores: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2962943/ https://ncbi.nlm.nih.gov/pubmed/20088824 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BJ20091641 |
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