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...

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Detalles Bibliográficos
Autores principales: Xia, Guangbin, Terada, Naohiro, Ashizawa, Tetsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
In Vitro and In Vivo Models in Stem Cell Biology (E Scott, Section Editor)
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

Internet

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

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