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

Abstract 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...

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Bibliographic Details
Main Authors: Roy W. R. Dudley, Alain S. Comtois, David H. St‐Pierre, Gawiyou Danialou
Format: Article
Language:English
Published: Wiley 2021-08-01
Series:FASEB BioAdvances
Subjects:
mdx
Online Access:https://doi.org/10.1096/fba.2020-00104