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Human iPSC Models to Study Orphan Diseases: Muscular Dystrophies
PURPOSE OF REVIEW: Muscular dystrophies (MDs) are a spectrum of muscle disorders, which are caused by a number of gene mutations. The studies of MDs are limited due to lack of appropriate models, except for Duchenne muscular dystrophy (DMD), myotonic dystrophy type 1 (DM1), facioscapulohumeral muscu...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Springer International Publishing
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244555/ https://www.ncbi.nlm.nih.gov/pubmed/30524939 http://dx.doi.org/10.1007/s40778-018-0145-5 |