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Brief Report

C9orf72 repeat expansions are not detected in Chinese patients with familial ALS

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Pages 630-631 | Received 28 Apr 2013, Accepted 15 Jun 2013, Published online: 22 Jul 2013

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. (2019) Theme 2 Genetics and genomics. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 20:sup1, pages 114-134.
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Articles from other publishers (15)

Lu Tang, Lu Chen, Xiaolu Liu, Ji He, Yan Ma, Nan Zhang & Dongsheng Fan. (2022) The repeat length of C9orf72 is associated with the survival of amyotrophic lateral sclerosis patients without C9orf72 pathological expansions. Frontiers in Neurology 13.
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Xiaolu Liu, Ji He, Lu Chen, Nan Zhang, Lu Tang, Xiangyi Liu, Yan Ma & Dongsheng Fan. (2021) TBK1 variants in Chinese patients with amyotrophic lateral sclerosis. Neurobiology of Aging 97, pages 149.e9-149.e15.
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Lu Tang, Yan Ma, Xiao-lu Liu, Lu Chen & Dong-sheng Fan. (2019) Better survival in female SOD1-mutant patients with ALS: a study of SOD1-related natural history. Translational Neurodegeneration 8:1.
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Xiangyi Liu, Chujun Wu, Ji He, Nan Zhang & Dongsheng Fan. (2019) Two rare variants of the ANXA11 gene identified in Chinese patients with amyotrophic lateral sclerosis. Neurobiology of Aging 74, pages 235.e9-235.e12.
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Kang Zhang, Qing Liu, Dongchao Shen, Hongfei Tai, Shuangwu Liu, Zhili Wang, Jiayu Shi, Hanhui Fu, Shuang Wu, Qingyun Ding, Youfang Hu, Yimin Wu, Xiaoguang Li, Yuzhou Guan, Mingsheng Liu, Liying Cui & Xue Zhang. (2019) Mutation analysis of KIF5A in Chinese amyotrophic lateral sclerosis patients. Neurobiology of Aging 73, pages 229.e1-229.e4.
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Danyang Tian, Jiao Li, Lu Tang, Nan Zhang & Dongsheng Fan. (2018) Screening for CCNF Mutations in a Chinese Amyotrophic Lateral Sclerosis Cohort. Frontiers in Aging Neuroscience 10.
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Kang Zhang, Qing Liu, Dongchao Shen, Hongfei Tai, Hanhui Fu, Shuangwu Liu, Jinyi Chen, Xiaoguang Li, Mingsheng Liu, Xue Zhang & Liying Cui. (2018) Screening of GLE1 mutations in Chinese amyotrophic lateral sclerosis patients. Neurobiology of Aging 66, pages 178.e9-178.e11.
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Lianping Xu, Jiao Li, Danyang Tian, Lu Chen, Lu Tang & Dongsheng Fan. (2018) The rs696880 Polymorphism in the Nogo-A Receptor Gene (RTN4R) Is Associated With Susceptibility to Sporadic Amyotrophic Lateral Sclerosis in the Chinese Population. Frontiers in Aging Neuroscience 10.
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Zhang-Yu Zou, Zhi-Rui Zhou, Chun-Hui Che, Chang-Yun Liu, Rao-Li He & Hua-Pin Huang. (2017) Genetic epidemiology of amyotrophic lateral sclerosis: a systematic review and meta-analysis. Journal of Neurology, Neurosurgery & Psychiatry 88:7, pages 540-549.
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N Shahrizaila, G Sobue, S Kuwabara, S H Kim, Carol Birks, D S Fan, J S Bae, C J Hu, M Gourie-Devi, Y Noto, K Shibuya, K J Goh, R Kaji, CP Tsai, L Cui, P Talman, R D Henderson, S Vucic & M C Kiernan. (2016) Amyotrophic lateral sclerosis and motor neuron syndromes in Asia. Journal of Neurology, Neurosurgery & Psychiatry 87:8, pages 821-830.
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Xijia Xu, Shiping Xie, Xiaomeng Shi, Jie Lv, Xiaowei Tang, Xiaolan Wang, Shuiping Lu, Mingzhong Wang, Xiaobing Zhang, Jing Sun & Hui Yao. (2015) Hexanucleotide Repeat Expansion in C9ORF72 Is Not Detected in the Treatment-Resistant Schizophrenia Patients of Chinese Han. PLOS ONE 10:12, pages e0145347.
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Ji He, Lu Tang, Beben Benyamin, Sonia Shah, Gib Hemani, Rong Liu, Shan Ye, Xiaolu Liu, Yan Ma, Huagang Zhang, Katie Cremin, Paul Leo, Naomi R. Wray, Peter M. Visscher, Huji Xu, Matthew A. Brown, Perry F. Bartlett, Marie Mangelsdorf & Dongsheng Fan. (2015) C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis. Neurobiology of Aging 36:9, pages 2660.e1-2660.e8.
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Zhi-Jun Liu, Hong-Fu Li, Guo-He Tan, Qing-Qing Tao, Wang Ni, Xue-Wen Cheng, Zhi-Qi Xiong & Zhi-Ying Wu. (2014) Identify mutation in amyotrophic lateral sclerosis cases using HaloPlex target enrichment system. Neurobiology of Aging 35:12, pages 2881.e11-2881.e15.
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Sabina Vatovec, Anja Kovanda & Boris Rogelj. (2014) Unconventional features of C9ORF72 expanded repeat in amyotrophic lateral sclerosis and frontotemporal lobar degeneration. Neurobiology of Aging 35:10, pages 2421.e1-2421.e12.
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Ione O. C. Woollacott & Simon Mead. (2014) The C9ORF72 expansion mutation: gene structure, phenotypic and diagnostic issues. Acta Neuropathologica 127:3, pages 319-332.
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