Spinocerebellar Ataxia Type 6
Author:
Publisher
Elsevier
Reference66 articles.
1. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias: A study of 11 families, including descendants of ‘Drew family of Walworth—;Harding;Brain,1982
2. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the a1A voltage-dependent calcium channel;Zhuchenko;Nat. Genet.,1997
3. Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1;Ishikawa;Am. J. Hum. Genet.,1997
4. Spinocerebellar ataxia type 6. Molecular and clinical features of 35 Japanese patients including one homozygous for the CAG repeat expansion;Matsumura;Neurology,1997
5. Frequency analysis of autosomal dominant cerebellar ataxias in Japanese patients and clinical characterization of spinocerebellar ataxia type 6;Watanabe;Clin. Genet.,1998
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