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