Current Understanding of Molecular Pathology and Treatment of Cardiomyopathy in Duchenne Muscular Dystrophy

Duchenne muscular dystrophy (DMD) is a genetic muscle disorder caused by mutations in the Dmd gene resulting in the loss of the protein dystrophin. Patients do not only experience skeletal muscle degeneration, but also develop severe cardiomyopathy by their second decade, one of the main causes of d...

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Detalles Bibliográficos
Autores principales: van Westering, Tirsa L. E., Betts, Corinne A., Wood, Matthew J. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272314/
https://www.ncbi.nlm.nih.gov/pubmed/25988613
http://dx.doi.org/10.3390/molecules20058823

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272314/
https://www.ncbi.nlm.nih.gov/pubmed/25988613
http://dx.doi.org/10.3390/molecules20058823

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