Frequency analysis of autosomal dominant cerebellar ataxias in Japanese patients and clinical characterization of spinocerebellar ataxia type 6
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1998.tb02575.x/fullpdf
Reference32 articles.
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2. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1;Orr;Nature Genet,1993
3. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2;Pulst;Nature Genet,1996
4. Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique DIRECT;Sanpei;Nature Genet,1996
5. Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats;Imbert;Nature Genet,1996
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