Clinical behaviour of spinocerebellar ataxia type 12 and intermediate length abnormal CAG repeats inPPP2R2B
Author:
Publisher
Oxford University Press (OUP)
Subject
Neurology (clinical)
Link
http://academic.oup.com/brain/article-pdf/140/1/27/10411370/aww269.pdf
Reference27 articles.
1. Evidence of a Common Founder for SCA12 in the Indian Population
2. Spinocerebellar ataxia type 12 identified in two Italian families may mimic sporadic ataxia;Brussino;Mov Disord,2010
3. Identification of 46 CAG repeats within PPP2R2B as probably the shortest pathogenic allele for SCA12;Dong;Parkinsonism Relat Disord,2015
4. Molecular pathogenesis of spinocerebellar ataxias
5. SCA-LSVD: A repeat-oriented locus-specific variation database for genotype to phenotype correlations in spinocerebellar ataxias
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