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Dysferlin-deficient immortalized human myoblasts and myotubes as a useful tool to study dysferlinopathy
Dysferlin gene mutations causing LGMD2B are associated with defects in muscle membrane repair. Four stable cell lines have been established from primary human dysferlin-deficient myoblasts harbouring different mutations in the dysferlin gene. We have compared immortalized human myoblasts and myotube...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3274833/ https://ncbi.nlm.nih.gov/pubmed/22367358 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/currents.RRN1298 |
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