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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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| Publicado no: | Eur Heart J Case Rep |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2019
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| Assuntos: | |
| Acesso em linha: | 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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