Early administration of L‐arginine in mdx neonatal mice delays the onset of muscular dystrophy in tibialis anterior (TA) muscle

Duchenne muscular dystrophy (DMD) is a genetic disorder that results in the absence of dystrophin, a cytoskeletal protein. Individuals with this disease experience progressive muscle destruction, which leads to muscle weakness. Studies have been conducted to find solutions for the relief of individu...

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Detalles Bibliográficos
Autores principales: Dudley, Roy W. R., Comtois, Alain S., St‐Pierre, David H., Danialou, Gawiyou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8332474/
https://www.ncbi.nlm.nih.gov/pubmed/34377959
http://dx.doi.org/10.1096/fba.2020-00104

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8332474/
https://www.ncbi.nlm.nih.gov/pubmed/34377959
http://dx.doi.org/10.1096/fba.2020-00104

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