Author:
Wang Yin-guang,Du Juan,Wang Jun-ling,Chen Juan,Chen Chong,Luo Ying-ying,Xiao Zhi-quan,Jiang Hong,Yan Xin-xiang,Xia Kun,Pan Qian,Tang Bei-sha,Shen Lu
Subject
Neurology (clinical),Neurology
Reference22 articles.
1. Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds;Tang;Arch Neurol,2000
2. Dominantly inherited ataxias: lessons learned from Machado–Joseph disease/spinocerebellar ataxia type 3;Paulson;Semin Neurol,2007
3. New insights into the pathoanatomy of spinocerebellar ataxia type 3 (Machado–Joseph disease);Rüb;Curr Opin Neurol,2008
4. SCA3: neurological features, pathogenesis and animal models;Riess;Cerebellum,2008
5. Machado–Joseph disease: a proposal of spastic paraplegic subtype;Sakai;Neurology,1996
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