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Huntingtin gene CAG repeat numbers in Chinese patients with Huntington's disease and controls

✍ Scribed by Jiang, H.; Sun, Y. M.; Hao, Y.; Yan, Y. P.; Chen, K.; Xin, S. H.; Tang, Y. P.; Li, X. H.; Jun, T.; Chen, Y. Y.; Liu, Z. J.; Wang, C. R.; Li, H.; Pei, Z.; Shang, H. F.; Zhang, B. R.; Gu, W. H.; Wu, Z. Y.; Tang, B. S.; Burgunder, J.-M.


Book ID
127084164
Publisher
John Wiley and Sons
Year
2014
Tongue
English
Weight
837 KB
Volume
21
Category
Article
ISSN
1351-5101

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Trinucleotide (CAG) repeat expansion in
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Huntington's disease (HD) is a neurodegenerative and hereditary disease characterized by progressive movement disorders and mental and behavioral abnormalities. The HD gene is an expanding and unstable trinucleotide repeat (CAG repeat sequences). We studied 77 individuals from 38 families with HD in