Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease-Reference-Cited by-同舟云学术

Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease

Published:2004-01-30 Issue:3 Volume:65 Page:209-214
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Wu YR,Lin HY,Chen CM,Gwinn-Hardy K,Ro LS,Wang YC,Li SH,Hwang JC,Fang K,Hsieh-Li HM,Li ML,Tung LC,Su MT,Lu KT,Lee-Chen GJ

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference48 articles.

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2. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2;Pulst;Nat Genet,1996

3. CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1;Kawaguchi;Nat Genet,1994

4. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel;Zhuchenko;Nat Genet,1997

5. Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion;David;Nat Genet,1997

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