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...

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Detalles Bibliográficos
Autores principales: Rugowska, Anna, Starosta, Alicja, Konieczny, Patryk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Review
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

Internet

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

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