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Striatal dopamine and homovanillic acid in Huntington's Disease

✍ Scribed by G. P. Reynolds; N. J. Garrett


Publisher
Springer
Year
1986
Tongue
English
Weight
246 KB
Volume
65
Category
Article
ISSN
1435-1463

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## Abstract Huntington's disease (HD) is a progressive neurodegenerative disorder caused by an expanded CAG repeat region in exon 1 of the HD gene. This mutation results in the presence of an abnormally long polyglutamine tract in the encoded protein, huntingtin (htt). A major question in this fiel