Carregant...
Targeting muscle stem cell intrinsic defects to treat Duchenne muscular dystrophy
Duchenne muscular dystrophy (DMD) is a genetic disease characterised by skeletal muscle degeneration and progressive muscle wasting, which is caused by loss-of-function mutations in the DMD gene that encodes for the protein dystrophin. Dystrophin has critical roles in myofiber stability and integrit...
Guardat en:
| Publicat a: | NPJ Regen Med |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Nature Publishing Group
2016
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5703417/ https://ncbi.nlm.nih.gov/pubmed/29188075 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/npjregenmed.2016.6 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|