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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| Publicado no: | J Clin Invest |
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| Principais autores: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Clinical Investigation
2002
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| Assuntos: | |
| Acesso em linha: | 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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