Expanded Triple Repeat
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-55065-7_33
Reference13 articles.
1. Brook, J. D., McCurrach, M. E., Harley, H. G., et al. (1992). 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(4), 799–808.
2. Di Prospero, N. A., & Fischbeck, K. H. (2005). Therapeutics development for triplet repeat expansion diseases. Nature Reviews Genetics, 6(10), 756–767.
3. Farmer, T. W., Wingfield, M. S., Lynch, S. A., Vogel, F. S., Hulette, C., Katchinoff, B., & Jacobson, P. L. (1989). Ataxia, chorea, seizures, and dementia: Pathologic features of a newly defined familial disorder. Archives of Neurology, 46(7), 774–779.
4. Kennedy, W. R., Alter, M., & Sung, J. H. (1998). Progressive proximal spinal and bulbar muscular atrophy of late onset. A sex-linked recessive trait. Neurology, 50(3), 583–583.
5. La Spada, A. R., & Wilson, E. M. (1991). Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature, 352(6330), 77.
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