Modeling Duchenne Muscular Dystrophy Cardiomyopathy with Patients’ Induced Pluripotent Stem-Cell-Derived Cardiomyocytes

Duchenne muscular dystrophy (DMD) is an X-linked progressive muscle degenerative disease caused by mutations in the dystrophin gene, resulting in death by the end of the third decade of life at the latest. A key aspect of the DMD clinical phenotype is dilated cardiomyopathy, affecting virtually all...

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Detalles Bibliográficos
Autores principales: Eisen, Binyamin, Binah, Ofer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10218670/
https://www.ncbi.nlm.nih.gov/pubmed/37240001
http://dx.doi.org/10.3390/ijms24108657

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10218670/
https://www.ncbi.nlm.nih.gov/pubmed/37240001
http://dx.doi.org/10.3390/ijms24108657

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