Analysis of trinucleotide repeats in different SCA loci in spinocerebellar ataxia patients and in normal population of Taiwan
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology,General Medicine
Reference37 articles.
1. THE CLINICAL FEATURES AND CLASSIFICATION OF THE LATE ONSET AUTOSOMAL DOMINANT CEREBELLAR ATAXIAS
2. Autosomal dominant cerebellar ataxia: Phenotypic differences in genetically defined subtypes?
3. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
4. Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats
5. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2
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