Sporadic SCA8 mutation resembling corticobasal degeneration
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference17 articles.
1. An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8);Koob;Nat Genet,1999
2. Long repeat tracts at SCA8 in major psychosis;Vincent;Am J Med Genet,2000
3. Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Italy;Cellini;Arch Neurol,2001
4. Molecular and clinical analyses of spinocerebellar ataxia type 8 in Japan;Ikeda;Neurology,2000
5. SCA8 repeat expansion: large CTA/CTG repeat alleles are more common in ataxic patients, including those with SCA6;Izumi;Am J Hum Genet,2003
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