Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHP
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng0897-402.pdf
Reference31 articles.
1. Brook, J.D. et al. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member. Cell 68, 799–808 (1992).
2. Fu, Y.H. et al. An unstable triplet repeat in a gene related to myotonic dystrophy. Science 255, 1256–1258 (1992).
3. Mahadevan, M. et al. Myotonic dystrophy: an unstable CTG repeat in the 3′ untranslated region of the gene. Science 255, 1253–1255 (1992).
4. Harris, S., Moncrieff, C. & Johnson, K. Myotonic dystrophy: will the real gene please step forward! . Hum Mol. Genet. 5, 1417–1423 (1996).
5. Otten, A.D. & Tapscott, S.J. Triplet repeat expansion in myotonic dystrophy alters the adjacent chromatin structure. Proc. Natl. Acad. Sci. USA 92, 5465–5469 (1995).
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