Perspectives on hiPSC-Derived Muscle Cells as Drug Discovery Models for Muscular Dystrophies

Muscular dystrophies are a heterogeneous group of inherited diseases characterized by the progressive degeneration and weakness of skeletal muscles, leading to disability and, often, premature death. To date, no effective therapies are available to halt or reverse the pathogenic process, and meaning...

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Detalles Bibliográficos
Autores principales: Abati, Elena, Sclarandi, Emanuele, Comi, Giacomo Pietro, Parente, Valeria, Corti, Stefania
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8431796/
https://www.ncbi.nlm.nih.gov/pubmed/34502539
http://dx.doi.org/10.3390/ijms22179630

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8431796/
https://www.ncbi.nlm.nih.gov/pubmed/34502539
http://dx.doi.org/10.3390/ijms22179630

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