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Dysferlin at transverse tubules regulates Ca(2+) homeostasis in skeletal muscle

The class of muscular dystrophies linked to the genetic ablation or mutation of dysferlin, including Limb Girdle Muscular Dystrophy 2B (LGMD2B) and Miyoshi Myopathy (MM), are late-onset degenerative diseases. In lieu of a genetic cure, treatments to prevent or slow the progression of dysferlinopathy...

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Bibliografiske detaljer
Main Authors: Kerr, Jaclyn P., Ward, Christopher W., Bloch, Robert J.
Format: Artigo
Sprog:Inglês
Udgivet: Frontiers Media S.A. 2014
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3944681/
https://ncbi.nlm.nih.gov/pubmed/24639655
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2014.00089
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