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Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration Volume 17, 2016 - Issue 5-6
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Research Article

CHCHD10 is not a frequent causative gene in Chinese ALS patients

Xiao Ling LiDepartment of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College, Beijing, ;McKusick-Zhang Centre for Genetic Medicine, CAMS & PUMC, Beijing, China
,
Shi ShuDepartment of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College, Beijing, ;Neuroscience Center, CAMS Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, and ;McKusick-Zhang Centre for Genetic Medicine, CAMS & PUMC, Beijing, China
,
Xiao Guang LiDepartment of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College, Beijing, Correspondence[email protected]
,
Qing LiuDepartment of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College, Beijing, ;Neuroscience Center, CAMS Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, and
,
Fang LiuDepartment of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College, Beijing, ;McKusick-Zhang Centre for Genetic Medicine, CAMS & PUMC, Beijing, China
,
Bo CuiDepartment of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College, Beijing,
,
Ming Sheng LiuDepartment of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College, Beijing,
,
Bin PengDepartment of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College, Beijing,
,
Li Ying CuiDepartment of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College, Beijing, ;Neuroscience Center, CAMS Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, and Correspondence[email protected]
&
Xue ZhangDepartment of Neurology and Laboratory of Clinical Genetics, Peking Union Medical College, Beijing, ;Neuroscience Center, CAMS Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College (CAMS & PUMC), Beijing, and ;McKusick-Zhang Centre for Genetic Medicine, CAMS & PUMC, Beijing, China
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Pages 458-460 | Received 28 Jan 2016, Accepted 24 Feb 2016, Published online: 14 Apr 2016

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Yaling Jiang, Bin Jiao, Xuewen Xiao & Lu Shen. (2021) Genetics of frontotemporal dementia in China. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 22:5-6, pages 321-335.
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Articles from other publishers (8)

Michele Longoni Calió, Elisandra Henriques, Amanda Siena, Clélia Rejane Antonio Bertoncini, Joana Gil-Mohapel & Tatiana Rosado Rosenstock. (2020) Mitochondrial Dysfunction, Neurogenesis, and Epigenetics: Putative Implications for Amyotrophic Lateral Sclerosis Neurodegeneration and Treatment. Frontiers in Neuroscience 14.
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Emily P McCann, Jennifer A Fifita, Natalie Grima, Jasmin Galper, Prachi Mehta, Sarah E Freckleton, Katharine Y Zhang, Lyndal Henden, Alison L Hogan, Sandrine Chan Moi Fat, Sharlynn SL Wu, Cyril J Jagaraj, Britt A Berning, Kelly Louise Williams, Natalie A Twine, Denis Bauer, Olivier Piguet, John Hodges, John B J Kwok, Glenda M Halliday, Matthew C Kiernan, Julie Atkin, Dominic B Rowe, Garth A Nicholson, Adam K Walker, Ian P Blair & Shu Yang. (2020) Genetic and immunopathological analysis of CHCHD10 in Australian amyotrophic lateral sclerosis and frontotemporal dementia and transgenic TDP-43 mice. Journal of Neurology, Neurosurgery & Psychiatry 91:2, pages 162-171.
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Jemeen Sreedharan, Iona Blakeney & Robert H. Brown. 2020. Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease. Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease 321 344 .
Mariana Dutra Brito, Gustavo Ferro Gomes da Silva, Erick Mutti Tilieri, Beatriz Grisolia Araujo, Michele Longoni Calió & Tatiana Rosado Rosenstock. (2019) Metabolic Alteration and Amyotrophic Lateral Sclerosis Outcome: A Systematic Review. Frontiers in Neurology 10.
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Xiaolu Liu, Ji He, Fen-Biao Gao, Aaron D. Gitler & Dongsheng Fan. (2018) The epidemiology and genetics of Amyotrophic lateral sclerosis in China. Brain Research 1693, pages 121-126.
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Neeraja Purandare, Mallika Somayajulu, Maik Hüttemann, Lawrence I. Grossman & Siddhesh Aras. (2018) The cellular stress proteins CHCHD10 and MNRR1 (CHCHD2): Partners in mitochondrial and nuclear function and dysfunction. Journal of Biological Chemistry 293:17, pages 6517-6529.
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Shen Shen, Ji He, Lu Tang, Nan Zhang & Dongsheng Fan. (2017) CHCHD10 mutations in patients with amyotrophic lateral sclerosis in Mainland China. Neurobiology of Aging 54, pages 214.e7-214.e10.
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Matthew A. White & Jemeen Sreedharan. (2016) Amyotrophic lateral sclerosis: recent genetic highlights. Current Opinion in Neurology 29:5, pages 557-564.
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