Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysis
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0404.2005.00400.x/fullpdf
Reference49 articles.
1. THE CLINICAL FEATURES AND CLASSIFICATION OF THE LATE ONSET AUTOSOMAL DOMINANT CEREBELLAR ATAXIAS
2. CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia
3. Identification of a novel SCA locus ( SCA19 ) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21
4. A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1
5. A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21‐q23
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