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De novo expansion of a CAG repeat in a Japanese patient with sporadic Huntington’s disease

✍ Scribed by Masahiko Watanabe; Akiko Satoh; Mizuki Kanemoto; Norio Ohkoshi; Shin’ichi Shoji

Book ID
119465189
Publisher
Elsevier Science
Year
2000
Tongue
English
Weight
87 KB
Volume
178
Category
Article
ISSN
0022-510X

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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