Reversible cardiac disease features in an inducible CUG repeat RNA–expressing mouse model of myotonic dystrophy
Author:
Funder
National Institutes of Health
Muscular Dystrophy Association
Myotonic Dystrophy Foundation
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Link
https://insight.jci.org/articles/view/143465/files/pdf
Reference74 articles.
1. The myotonic dystrophies: diagnosis and management
2. Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member
3. Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the Gene
4. RNA toxicity in human disease and animal models: from the uncovering of a new mechanism to the development of promising therapies;Sicot;Biochim Biophys Acta,2013
5. Expansion of a CUG trinucleotide repeat in the 3' untranslated region of myotonic dystrophy protein kinase transcripts results in nuclear retention of transcripts
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