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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Detalles Bibliográficos
Autores principales: Philippi, Susanne, Bigot, Anne, Marg, Andreas, Mouly, Vincent, Spuler, Simone, Zacharias, Ute
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Muscular Dystrophy
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3274833/
https://www.ncbi.nlm.nih.gov/pubmed/22367358
http://dx.doi.org/10.1371/currents.RRN1298

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3274833/
https://www.ncbi.nlm.nih.gov/pubmed/22367358
http://dx.doi.org/10.1371/currents.RRN1298

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