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Genetic Manipulation of Dysferlin Expression in Skeletal Muscle : Novel Insights into Muscular Dystrophy

Mutations in the gene DYSF, which codes for the protein dysferlin, underlie Miyoshi myopathy and limb-girdle muscular dystrophy 2B in humans and produce a slowly progressing skeletal muscle degenerative disease in mice. Dysferlin is a Ca(2+)-sensing, regulatory protein that is involved in membrane r...

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Detalhes bibliográficos
Main Authors: Millay, Douglas P., Maillet, Marjorie, Roche, Joseph A., Sargent, Michelle A., McNally, Elizabeth M., Bloch, Robert J., Molkentin, Jeffery D.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Investigative Pathology 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2774048/
https://ncbi.nlm.nih.gov/pubmed/19834057
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/ajpath.2009.090107
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