Reduction in Size of the Myotonic Dystrophy Trinucleotide Repeat Mutation During Transmission
Author:
Affiliation:
1. Department of Microbiology and Immunology, University of Ottawa, Canada K1 H 8M5.
2. Division of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Canada K1 H 8L1.
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference25 articles.
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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. FU, Y.H., CELL 67: 1 (1991).
4. An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular Dystrophy
5. Harper P. S. Myotonic Dystrophy 2 (1989).
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