Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Syndrome and ATP13A2[original query] |
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ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease. Neurology 2007 May 68 (19): 1557-62. Di Fonzo A, Chien H F, Socal M, Giraudo S, Tassorelli C, Iliceto G, Fabbrini G, Marconi R, Fincati E, Abbruzzese G, Marini P, Squitieri F, Horstink M W, Montagna P, Libera A Dalla, Stocchi F, Goldwurm S, Ferreira J J, Meco G, Martignoni E, Lopiano L, Jardim L B, Oostra B A, Barbosa E R, , Bonifati |
ATP13A2 variability in Parkinson disease. Human mutation 2009 Mar 30 (3): 406-10. Vilariño-Güell Carles, Soto Alexandra I, Lincoln Sarah J, Ben Yahmed Samia, Kefi Mounir, Heckman Michael G, Hulihan Mary M, Chai Hua, Diehl Nancy N, Amouri Rim, Rajput Alex, Mash Deborah C, Dickson Dennis W, Middleton Lefkos T, Gibson Rachel A, Hentati Faycal, Farrer Matthew |
ATP13A2 variants in early-onset Parkinson's disease patients and controls. Movement disorders : official journal of the Movement Disorder Society 2009 Oct 24 (14): 2104-11. Djarmati Ana, Hagenah Johann, Reetz Kathrin, Winkler Susen, Behrens Maria Isabel, Pawlack Heike, Lohmann Katja, Ramirez Alfredo, Tadi? Vera, Brüggemann Norbert, Berg Daniela, Siebner Hartwig R, Lang Anthony E, Pramstaller Peter P, Binkofski Ferdinand, Kosti? Vladimir S, Volkmann Jens, Gasser Thomas, Klein Christi |
Lack of association between ATP13A2 Ala746Thr variant and Parkinson's disease in Han population of mainland China. Neuroscience letters 2010 May 475 (2): 61-3. Fei Qing-Zhou, Cao Li, Xiao Qin, Zhang Ting, Zheng Lan, Wang Xi-Jin, Wang Gang, Zhou Hai-Yan, Wang Ying, Chen Sheng- |
The role of the Ala746Thr variant in the ATP13A2 gene among Chinese patients with Parkinson's disease. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2013 May 20 (5): 761-2. Chan Anne Y Y, Baum Larry, Tang Nelson L S, Lau Christine Y K, Ng Ping Wing, Hui Kwok Fai, Mizuno Yoshi, Kwan Justin Y, Mok Vincent C T, Kuo Sheng-H |
Genetic analysis of ATP13A2, PLA2G6 and FBXO7 in a cohort of Chinese patients with early-onset Parkinson's disease. Scientific reports 2018 Sep 8 (1): 14028. Shen Ting, Pu Jiali, Lai Hsin-Yi, Xu Lingjia, Si Xiaoli, Yan Yaping, Jiang Yasi, Zhang Baoro |
Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysis. American journal of medical genetics. Part A 2022 Sep . Kumar Runjun D, Meng Linyan, Liu Pengfei, Miyake Christina Y, Worley Kim C, Bi Weimin, Lalani Seema |
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