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Reduction of the Rate of Protein Translation in Patients with Myotonic Dystrophy 2
Myotonic dystrophy 2 (DM2) is an autosomal dominant, multisystem disease, which primarily affects skeletal muscle. DM2 is caused by CCTGn expansion in the intron 1 of the ZNF9 gene. Expression of the mutant CCUGn RNA changes RNA processing in patients with DM2; however, the role of ZNF9 protein in D...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Society for Neuroscience
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3610333/ https://ncbi.nlm.nih.gov/pubmed/19605641 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.1983-09.2009 |
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