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Hypersensitivity of excitation-contraction coupling in dystrophic cardiomyocytes
Duchenne muscular dystrophy represents a severe inherited disease of striated muscle. It is caused by a mutation of the dystrophin gene and characterized by a progressive loss of skeletal muscle function. Most patients also develop a dystrophic cardiomyopathy, resulting in dilated hypertrophy and he...
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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Physiological Society
2009
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3774091/ https://ncbi.nlm.nih.gov/pubmed/19783774 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpheart.00602.2009 |
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