Identification of five Spinocerebellar Ataxia Type 2 pedigrees in patients with autosomal dominant cerebellar ataxia in Taiwan
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0404.1999.tb00737.x/fullpdf
Reference28 articles.
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2. Autosomal dominant cerebellar phenotypes: the genotype will settle the issue;Rosenberg;Neurology,1990
3. Autosomal dominant cerebellar phenotypes: the genotype has settled the issue;Rosenberg;Neurology,1995
4. Expansion of an unstable trinucleotide CAG Repeat in spinocerebellar ataxia type 1;Orr;Nat Genet,1993
5. Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT;Sanpei;Nat Genet,1996
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1. Genetic profile and clinical characteristics of Chinese patients with spinocerebellar ataxia type 2: A multicenter experience over 10 years;European Journal of Neurology;2020-12
2. Nationwide Population-Based Epidemiologic Study on Cerebellar Ataxia in Taiwan;European Neurology;2011
3. Machado-Joseph shoe;Movement Disorders;2004-08-10
4. Analysis of trinucleotide repeats in different SCA loci in spinocerebellar ataxia patients and in normal population of Taiwan;Acta Neurologica Scandinavica;2004-05
5. Spinocerebellar Ataxia 2 (SCA2);Genetics of Movement Disorders;2003
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