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The Ins and Outs of a Polyglutamine Neurodegenerative Disease: Spinocerebellar Ataxia Type 1 (SCA1)

✍ Scribed by Harry T. Orr


Book ID
115641536
Publisher
Elsevier Science
Year
2000
Tongue
English
Weight
49 KB
Volume
7
Category
Article
ISSN
0969-9961

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The CAG repeat tract at the autosomal dominant spinocerebellar ataxia type 1 (SCA1) locus was analyzed in SCA1 families and French-Acadian, African-American, Caucasian, Greenland Inuit, and Thai populations. The normal alleles had 9-37 repeats, whereas disease alleles contained 44-64 repeats. The CA