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Activation of the MEF2 transcription factor in skeletal muscles from myotonic mice

Becker syndrome, a recessive nondystrophic myotonia caused by mutations in the chloride channel 1 gene (CLCN1), is characterized by delayed muscle relaxation after contraction. The ADR (arrested development of righting response) mouse is an animal model for Becker syndrome. Skeletal muscles from ADR...

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Bibliografische Detailangaben
Veröffentlicht in:J Clin Invest
Hauptverfasser: Wu, Hai, Olson, Eric N.
Format: Artigo
Sprache:Inglês
Veröffentlicht: American Society for Clinical Investigation 2002
Schlagworte:
Online-Zugang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC150985/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12021248/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI15417
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