Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK.-Reference-Cited by-同舟云学术

Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK.

Published:1997-12-01 Issue:12 Volume:34 Page:982-985
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Leggo J,Dalton A,Morrison P J,Dodge A,Connarty M,Kotze M J,Rubinsztein D C

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference26 articles.

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3. The expanding world of ataxins;Zoghbi, H.;Nat Genet,1996

4. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1;Orr, H.T.; Chung, M.; Banfi, S.,1993

5. CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1;Kawaguchi, Y.; Okamoto, T.; Taniwaki, M.,1994

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