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Reversible model of RNA toxicity and cardiac conduction defects in myotonic dystrophy
Myotonic dystrophy (DM1), the most common muscular dystrophy in adults, is caused by an expanded (CTG)(n) tract in the 3′ UTR of the gene encoding myotonic dystrophy protein kinase (DMPK)1, which results in nuclear entrapment of the ‘toxic’ mutant RNA and interacting RNA-binding proteins (such as MB...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2909745/ https://ncbi.nlm.nih.gov/pubmed/16878132 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng1857 |
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