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CUGBP1 overexpression in mouse skeletal muscle reproduces features of myotonic dystrophy type 1
The neuromuscular disease myotonic dystrophy type I (DM1) affects multiple organ systems with the major symptoms being severe muscle weakness, progressive muscle wasting and myotonia. The causative mutation in DM1 is a CTG repeat expansion in the 3′-untranslated region of the DM protein kinase (DMPK...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2928132/ https://ncbi.nlm.nih.gov/pubmed/20603324 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq277 |
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