Genetic mapping of a second myotonic dystrophy locus
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng0698_196.pdf
Reference17 articles.
1. Harper, P.S. Myotonic Dystrophy (W.B. Saunders, London, 1989)
2. Fu, Y.-H. et al. Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox. Cell 67, 1047–1058 (1991)
3. Buxton, J. et al. Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy. Nature 355, 547–548 (1992)
4. Harley, H.G. et al. Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy . Nature 355, 545–546 (1992)
5. 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)
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