Metabolomic Analyses Reveal Extensive Progenitor Cell Deficiencies in a Mouse Model of Duchenne Muscular Dystrophy

Duchenne muscular dystrophy (DMD) is a musculoskeletal disorder that causes severe morbidity and reduced lifespan. Individuals with DMD have an X-linked mutation that impairs their ability to produce functional dystrophin protein in muscle. No cure exists for this disease and the few therapies that...

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Detalles Bibliográficos
Autores principales: Joseph, Josiane, Cho, Dong Seong, Doles, Jason D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315702/
https://www.ncbi.nlm.nih.gov/pubmed/30282911
http://dx.doi.org/10.3390/metabo8040061

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315702/
https://www.ncbi.nlm.nih.gov/pubmed/30282911
http://dx.doi.org/10.3390/metabo8040061

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