Myotonic Dystrophy Is Associated with a Reduced Level of RNA from the DMWD Allele Adjacent to the Expanded Repeat
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/8/8/1491/1654850/8-8-1491.pdf
Reference20 articles.
1. Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member
2. An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular Dystrophy
3. Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the Gene
4. Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy
5. Six transcripts map within 200 kilobases of the myotonic dystrophy expanded repeat
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