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Hope, humanity, and Huntington's disease in Latin America

✍ Scribed by Burton, Adrian


Book ID
123281083
Publisher
The Lancet
Year
2013
Tongue
English
Weight
340 KB
Volume
12
Category
Article
ISSN
1474-4465

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## Abstract Huntington's Disease–like 2 (HDL2) is a progressive, autosomal dominant, neurodegenerative disorder with marked clinical and pathological similarities to Huntington's disease (HD). The causal mutation is a CTG/CAG expansion mutation on chromosome 16q24.3, in a variably spliced exon of j