Identification of a (CUG)n triplet repeat RNA-binding protein and its expression in myotonic dystrophy.
Myotonic dystrophy (DM) is an autosomal dominant neuromuscular disease that is associated with a (CTG)n repeat expansion in the 3'-untranslated region of the myotonin protein kinase (Mt-PK) gene. This study reports the isolation and characterization of a (CUG)n triplet repeat pre-mRNA/mRNA binding p...
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| Veröffentlicht in: | Nucleic Acids Res |
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| Hauptverfasser: | , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Oxford University Press
1996
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| Schlagworte: | |
| Online-Zugang: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC146274/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8948631/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/24.22.4407 |
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