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Six cases of SCA3/MJD patients that mimic hereditary spastic paraplegia in clinic.
Wang YG, Du J, Wang JL, Chen J, Chen C, Luo YY, Xiao ZQ, Jiang H, Yan XX, Xia K, Pan Q, Tang BS, Shen L. Wang YG, et al. J Neurol Sci. 2009 Oct 15;285(1-2):121-4. doi: 10.1016/j.jns.2009.06.027. Epub 2009 Jul 15. J Neurol Sci. 2009. PMID: 19608203
[Recent advances of study on hereditary spastic paraplegia type 11].
Du J, Shen L, Tang B. Du J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Dec;26(6):670-3. doi: 10.3760/cma.j.issn.1003-9406.2009.06.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19953491 Review. Chinese.
TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.
Wang JL, Yang X, Xia K, Hu ZM, Weng L, Jin X, Jiang H, Zhang P, Shen L, Guo JF, Li N, Li YR, Lei LF, Zhou J, Du J, Zhou YF, Pan Q, Wang J, Wang J, Li RQ, Tang BS. Wang JL, et al. Brain. 2010 Dec;133(Pt 12):3510-8. doi: 10.1093/brain/awq323. Epub 2010 Nov 23. Brain. 2010. PMID: 21106500
Expansion of the phenotypic spectrum of SPG6 caused by mutation in NIPA1.
Du J, Hu YC, Tang BS, Chen C, Luo YY, Zhan ZX, Zhao GH, Jiang H, Xia K, Shen L. Du J, et al. Clin Neurol Neurosurg. 2011 Jul;113(6):480-2. doi: 10.1016/j.clineuro.2011.02.011. Epub 2011 Mar 17. Clin Neurol Neurosurg. 2011. PMID: 21419568
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