Expanded GAA repeats and clinical variation in Friedreich's ataxia
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1600-0404.2003.00190.x/fullpdf
Reference18 articles.
1. Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features;Harding;Brain,1981
2. Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion;Campuzano;Science,1996
3. Friedreich's ataxia presenting with pure sensory ataxia: a long-term follow-up study of two patients;Berciano;J Neurol,1993
4. Friedreich ataxia with minimal GAA expansion presenting as adult-onset spastic ataxia;Berciano;J Neurol Sci,2002
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