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Calcium homeostasis alterations in a mouse model of the Dynamin 2-related centronuclear myopathy

Autosomal dominant centronuclear myopathy (CNM) is a rare congenital myopathy characterized by centrally located nuclei in muscle fibers. CNM results from mutations in the gene encoding dynamin 2 (DNM2), a large GTPase involved in endocytosis, intracellular membrane trafficking, and cytoskeleton reg...

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Detalles Bibliográficos
Publicado en:Biol Open
Main Authors: Fraysse, Bodvaël, Guicheney, Pascale, Bitoun, Marc
Formato: Artigo
Idioma:Inglês
Publicado: The Company of Biologists Ltd 2016
Assuntos:
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5155535/
https://ncbi.nlm.nih.gov/pubmed/27870637
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/bio.020263
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