Zi X - Search Results

1

Mutation detection in candidate genes for benign familial infantile seizures on a novel locus.

Li N, Li H, Jiang H, Shen L, Yan X, Guo J, Song Y, Yang Q, Wang Y, Li X, Xiang R, Zi X, Long X, Hu Z, Pan Q, Xia K, Tang B. Li N, et al. Among authors: zi x. Int J Neurosci. 2010 Mar;120(3):217-21. doi: 10.3109/00207450903477779. Int J Neurosci. 2010. PMID: 20374090

2

A novel hemizygous SACS mutation identified by whole exome sequencing and SNP array analysis in a Chinese ARSACS patient.

Liu L, Li XB, Zi XH, Shen L, Hu ZhM, Huang ShX, Yu DL, Li HB, Xia K, Tang BS, Zhang RX. Liu L, et al. Among authors: zi xh. J Neurol Sci. 2016 Mar 15;362:111-4. doi: 10.1016/j.jns.2016.01.026. Epub 2016 Jan 18. J Neurol Sci. 2016. PMID: 26944128

3

[Mutation analysis of ganglioside-induced differentiation associated protein-1 gene in Chinese Charcot-Marie-Tooth disease].

Zhang RX, Tang BS, Zi XH, Luo W, Xia K, Pan Q, Long ZG, Hu ZM, Li XB. Zhang RX, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Jun;21(3):207-10. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15192818 Chinese.

4

Mutation screening of Cx32 in Han Chinese patients with Charcot-Marie-Tooth disease.

Zhang RX, Luo W, Zi XH, Xia K, Cai F, Xiao JF, Zhao GH, Zhang FF, Shen L, Jiang H, Tang BS. Zhang RX, et al. Beijing Da Xue Xue Bao Yi Xue Ban. 2005 Feb 18;37(1):68-71. Beijing Da Xue Xue Bao Yi Xue Ban. 2005. PMID: 15719046 Free article.

5

[Cloning to rule out 10 candidate genes located in chromosome 12q24 for Charcot-Marie-Tooth disease type 2L].

Zhang RX, Tang BS, Zi XH, Luo W, Xia K, Pan Q, Hu ZM, Zhao GH, Guo K. Zhang RX, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Apr;23(2):189-91. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16604494 Chinese.

6

[Mutation analysis of MFN2 gene in Chinese patients with Charcot-Marie-Tooth disease].

Zhang RX, Fu M, Zi XH, Li XB, Zhang FF, Xia K, Pan Q, Hu ZM, Tang BS. Zhang RX, et al. Zhonghua Yi Xue Za Zhi. 2009 Dec 22;89(47):3324-7. Zhonghua Yi Xue Za Zhi. 2009. PMID: 20193559 Chinese.

7

[Analysis of CX32 gene mutation and related clinical features in Chinese Han Charcot-Marie-Tooth families].

Zhan YJ, Zi XH, Li L, Li XB, Huang SX, Li L, Li XG, Hu ZM, Pan Q, Xia K, Tang BS, Zhang RX. Zhan YJ, et al. Zhonghua Yi Xue Za Zhi. 2012 Jun 5;92(21):1463-7. Zhonghua Yi Xue Za Zhi. 2012. PMID: 22944031 Chinese.

8

Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegia.

Tang B, Zhao G, Xia K, Pan Q, Luo W, Shen L, Long Z, Dai H, Zi X, Jiang H. Tang B, et al. Among authors: zi x. Arch Neurol. 2004 Jan;61(1):49-55. doi: 10.1001/archneur.61.1.49. Arch Neurol. 2004. PMID: 14732620

9

Two novel MPZ mutations in Chinese CMT patients.

Liu L, Li X, Zi X, Huang S, Zhan Y, Jiang M, Guo J, Xia K, Tang B, Zhang R. Liu L, et al. Among authors: zi x. J Peripher Nerv Syst. 2013 Sep;18(3):256-60. doi: 10.1111/jns5.12040. J Peripher Nerv Syst. 2013. PMID: 24028194

10

Zhan Y, Zi X, Hu Z, Peng Y, Wu L, Li X, Jiang M, Liu L, Xie Y, Xia K, Tang B, Zhang R. Zhan Y, et al. Among authors: zi x. Muscle Nerve. 2015 Jul;52(1):69-75. doi: 10.1002/mus.24550. Epub 2015 Mar 31. Muscle Nerve. 2015. PMID: 25522693

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