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Dystrophic Cardiomyopathy: Complex Pathobiological Processes to Generate Clinical Phenotype
Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), and X-linked dilated cardiomyopathy (XL-DCM) consist of a unique clinical entity, the dystrophinopathies, which are due to variable mutations in the dystrophin gene. Dilated cardiomyopathy (DCM) is a common complication of dystrophi...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715712/ https://www.ncbi.nlm.nih.gov/pubmed/29367543 http://dx.doi.org/10.3390/jcdd4030014 |