3ZHAO Y, LIM SW , TAN EK. Genetic analysis of SCA27 in ataxia and childhood onset postural tremor[J]. Am J Med Genet B Neuropsychiatr Genet, 2007, 144 ( 3 ) : 395 - 396.
4Dürr A, Stevanin G, Cancel G, et al. Spinoeerehellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuro- pathological features[J]. Ann Neurol, 1996, 39 (4): 490-499.
5Maciel P, Gaspar C, DeStefano AL, et al.Correlation between CAG repeat length and clinical features in Machado-Joseph disease[J]. AmJ Hum Genet,1995, 57(1): 54-57.
6Gan SR, Shi SS, Wu J J, et al. High frequency of Maehdo-Jo- seph disease identified in southeast chinese kingdreds with spi- nocerebellar ataxia[J]. BMC Med Genet, 2010, 11(1) :47-55.
7Tang B, Liu C, Shen L, et al. Frequency of SCAI,SCA2,SCA3/ MJD,SCA6,SCA7 and DRPLA CAG trinucleotide repeat expan- sion in patients with hereditary spinoeerebellar ataxia from Chi- nese Kindreds[J]. Arch Neurol, 2000, 57(4): 540-544.
8Ichikawa Y, Goto J, Hattori M, et al. The genomie structure and expression of MJD, the Maehado-Joseph disease gene[J]. J Hum Genet, 2001, 46 ( 3 ) :413-422.
9Maruyama H, Nakamura S, Matsuyama Z, et al. Molecular fea- tures of the CAG repeats and clinical manifestation of Machado- Joseph disease[J]. Hum Mol Genet, 1995, 4(8): 807-812.
10Warrick JM. Ataxin3 suppresses polyglutamine neurodegenera- tion in Drosophila by a ubiquitin- associated mechanism[J]. Mol Cell, 2005, 18(1) : 37-48.