Chinese patients with Huntington's disease initially presenting with spinocerebellar ataxia
Author:
Affiliation:
1. Department of Neurology and Institute of Neurology; Huashan Hospital, Institutes of Brain Science and State Key Laboratory of Medical Neurobiology, Shanghai Medical College, Fudan University; Shanghai; China
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2012.01927.x/fullpdf
Reference22 articles.
1. On Chorea;Huntington;Med Surg Rep,1872
2. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes;The Huntington's Disease Collaborative Research Group;Cell,1993
3. Trinucleotide repeat length instability and age of onset in Huntington's disease;Duyao;Nat Genet,1993
4. Atypical movement disorders in the early stages of Huntington's disease: clinical and genetic analysis;Squitieri;Clin Genet,2000
5. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1;Orr;Nat Genet,1993
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