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Autonomic, locomotor and cardiac abnormalities in a mouse model of muscular dystrophy: targeting the renin–angiotensin system

Muscular dystrophies are a heterogeneous group of genetic muscle diseases characterized by muscle weakness and atrophy. Mutations in sarcoglycans and other subunits of the dystrophin–glycoprotein complex cause muscular dystrophy and dilated cardiomyopathy in animals and humans. Aberrant autonomic si...

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Detalhes bibliográficos
Publicado no:Exp Physiol
Main Authors: Sabharwal, Rasna, Chapleau, MarkW.
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4322680/
https://ncbi.nlm.nih.gov/pubmed/24334334
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/expphysiol.2013.074336
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