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...
Guardat en:
| Publicat a: | J Clin Invest |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Clinical Investigation
2002
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| Matèries: | |
| Accés en línia: | 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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