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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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Publicat a:Nucleic Acids Res
Autors principals: Timchenko, L T, Miller, J W, Timchenko, N A, DeVore, D R, Datar, K V, Lin, L, Roberts, R, Caskey, C T, Swanson, M S
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 1996
Matèries:
Research Article
Accés en línia: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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