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A case report: X-linked dystrophin gene mutation causing severe isolated dilated cardiomyopathy
BACKGROUND : X-linked dilated cardiomyopathy (XLDCM) is a rare but rapidly progressive cardiomyopathy caused by dystrophin gene mutation. Mutations are more often associated with Duchenne and Becker Muscular Dystrophy, which are characterized by skeletal muscle weakness or limb girdle dystrophy. How...
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| Publicat a: | Eur Heart J Case Rep |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6601194/ https://ncbi.nlm.nih.gov/pubmed/31449615 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ehjcr/ytz055 |
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