Expanded‐repeat‐RNA ‐mediated disease mechanisms in myotonic dystrophy
Author:
Affiliation:
1. Department of Neurology Osaka University Graduate School of Medicine Osaka Japan
Funder
Japan Agency for Medical Research and Development
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/ncn3.12687
Reference68 articles.
1. Myotonic Dystrophy
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. An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular Dystrophy
4. Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the Gene
5. Myotonic Dystrophy in Transgenic Mice Expressing an Expanded CUG Repeat
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