Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Atrophy and ATXN8OS[original query] |
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[Studies on the CTA/CTG trinucleotide repeats of ATXN8OS gene in Chinese Hans]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2008 Oct 25 (5): 511-4. Wang Junling, Zhang Shen, Xu Qian, Li Xiaohui, Song Xingwang, Jiang Hong, Shen Lu, Yan Xinxiang, Pan Qian, Xia Kun, Tang Beis |
Noncoding repeat expansions for ALS in Japan are associated with the ATXN8OS gene. Neurology. Genetics 2018 8 4 (4): e252. Hirano Makito, Samukawa Makoto, Isono Chiharu, Saigoh Kazumasa, Nakamura Yusaku, Kusunoki Susu |
Frequency of spinocerebellar ataxia mutations in patients with multiple system atrophy. Clinical autonomic research : official journal of the Clinical Autonomic Research Society 2021 Jan . Wernick Anna I, Walton Ronald L, Soto-Beasley Alexandra I, Koga Shunsuke, Heckman Michael G, Valentino Rebecca R, Milanowski Lukasz M, Hoffman-Zacharska Dorota, Koziorowski Dariusz, Hassan Anhar, Uitti Ryan J, Cheshire William P, Singer Wolfgang, Wszolek Zbigniew K, Dickson Dennis W, Low Phillip A, Ross Owen |
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