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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Detalles Bibliográficos
Autores principales: Lester, Geoffrey, Femia, Giuseppe, Ayer, Julian, Puranik, Rajesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6601194/
https://www.ncbi.nlm.nih.gov/pubmed/31449615
http://dx.doi.org/10.1093/ehjcr/ytz055

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6601194/
https://www.ncbi.nlm.nih.gov/pubmed/31449615
http://dx.doi.org/10.1093/ehjcr/ytz055

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