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Dystrophin deficiency exacerbates skeletal muscle pathology in dysferlin-null mice
BACKGROUND: Mutations in the genes coding for either dystrophin or dysferlin cause distinct forms of muscular dystrophy. Dystrophin links the cytoskeleton to the sarcolemma through direct interaction with β-dystroglycan. This link extends to the extracellular matrix by β-dystroglycan's interact...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3287108/ https://ncbi.nlm.nih.gov/pubmed/22132688 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2044-5040-1-35 |
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