Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel-Reference-Cited by-同舟云学术

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel

Published:1997-01 Issue:1 Volume:15 Page:62-69
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Zhuchenko Olga,Bailey Jennifer,Bonnen Penelope,Ashizawa Tetsuo,Stockton David W.,Amos Chris,Dobyns William B.,Subramony S.H.,Zoghbi Huda Y.,Lee Cheng Chi

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0197-62.pdf

Reference45 articles.

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4. Orr, H. et al. Expansion of an unstable trinucleotide (CAG) repeat in spinocerebellarataxiatype. Nature Genet. 4, 221–226 (1993).

5. Pulst, S.M. et al. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. Nature Genet. . 14, 269–276 (1996).

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