Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Ataxia and COQ2[original query] |
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| Mutations in COQ2 in familial and sporadic multiple-system atrophy. The New England journal of medicine 2013 Jul 369 (3): 233-44. Authors are not available |
| Mutation scanning of the COQ2 gene in ethnic Chinese patients with multiple-system atrophy. Neurobiology of aging 2015 Feb 36 (2): 1222.e7-11. Chen Yong Ping, Zhao Bi, Cao Bei, Song Wei, Guo XiaoYan, Wei Qian-Qian, Yang Yuan, Yuan Li Xing, Shang Hui-Fa |
| Plasma Coenzyme Q10 Levels in Patients With Multiple System Atrophy. JAMA neurology 2016 Jun . Mitsui Jun, Matsukawa Takashi, Yasuda Tsutomu, Ishiura Hiroyuki, Tsuji Sho |
| New susceptible variant of COQ2 gene in Japanese patients with sporadic multiple system atrophy. Neurology. Genetics 2016 Apr 2 (2): e54. Sun Zhuoran, Ohta Yasuyuki, Yamashita Toru, Sato Kota, Takemoto Mami, Hishikawa Nozomi, Abe Ko |
| Reductions in COQ2 Expression Relate to Reduced ATP Levels in Multiple System Atrophy Brain. Frontiers in neuroscience 2019 13 1187. Hsiao Jen-Hsiang T, Purushothuman Sivaraman, Jensen Poul H, Halliday Glenda M, Kim Woojin Sco |
| COQ2 V393A confers high risk susceptibility for multiple system atrophy in East Asian population. Journal of the neurological sciences 2021 8 429 117623. Porto Kristine Joyce, Hirano Makito, Mitsui Jun, Chikada Ayaka, Matsukawa Takashi, Ishiura Hiroyuki, , Toda Tatsushi, Kusunoki Susumu, Tsuji Sho |
| Genetic profiles of multiple system atrophy revealed by exome sequencing, long-read sequencing and spinocerebellar ataxia repeat expansion analysis. European journal of neurology 2024 8 e16441. Xu-Ying Li, Hong Lai, Xian Li, Fanxi Xu, Yang Song, Zhanjun Wang, Qibin Li, Ruichai Lin, Zhiheng Xu, Chaodong Wa |
- Page last reviewed:Feb 1, 2024
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