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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Библиографические подробности
Главные авторы: Philippi, Susanne, Bigot, Anne, Marg, Andreas, Mouly, Vincent, Spuler, Simone, Zacharias, Ute
Формат: Artigo
Язык:Inglês
Опубликовано: Public Library of Science 2012
Предметы:
Muscular Dystrophy
Online-ссылка: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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