In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts
Myotonic dystrophy (DM1) is the most common form of adult muscular dystrophy and is inherited as an autosomal dominant trait. The genetic basis of DM1 is the expansion of a CTG repeat in the 3′ untranslated region of a protein kinase gene (DMPK). The molecular mechanism by which this expanded repeat...
Gardado en:
| Publicado en: | Nucleic Acids Res |
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| Principais autores: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Oxford University Press
2001
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC55763/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11433021/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/29.13.2766 |
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