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Calpain 3 is a modulator of the dysferlin protein complex in skeletal muscle

Muscular dystrophies comprise a genetically heterogeneous group of degenerative muscle disorders characterized by progressive muscle wasting and weakness. Two forms of limb-girdle muscular dystrophy, 2A and 2B, are caused by mutations in calpain 3 (CAPN3) and dysferlin (DYSF), respectively. While CA...

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Bibliografiske detaljer
Main Authors: Huang, Yanchao, de Morrée, Antoine, van Remoortere, Alexandra, Bushby, Kate, Frants, Rune R., Dunnen, Johan Tden, van der Maarel, Silvère M.
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2008
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2900895/
https://ncbi.nlm.nih.gov/pubmed/18334579
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn081
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