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Epigenetic modifications in muscle regeneration and progression of Duchenne muscular dystrophy
Duchenne muscular dystrophy (DMD) is a multisystemic disorder that affects 1:5000 boys. The severity of the phenotype varies dependent on the mutation site in the DMD gene and the resultant dystrophin expression profile. In skeletal muscle, dystrophin loss is associated with the disintegration of my...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7814631/ https://www.ncbi.nlm.nih.gov/pubmed/33468200 http://dx.doi.org/10.1186/s13148-021-01001-z |