Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Parkinson Disease and EIF4G1[original query] |
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VPS35 Asp620Asn and EIF4G1 Arg1205His mutations are rare in Parkinson disease from southwest China. Neurobiology of aging 2012 Dec . Chen Y, Chen K, Song W, Chen X, Cao B, Huang R, Zhao B, Guo X, Burgunder J, Li J, Shang HF |
EIF4G1 Ala502Val and Arg1205His variants in Chinese patients with Parkinson disease. Neuroscience letters 2013 May 543 69-71. Yuan Lamei, Song Zhi, Xu Hongbo, Gu Shaojuan, Zhu Anding, Gong Lina, Zhao Yongxiang, Deng H |
Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease. Neurology 2013 Mar 80 (11): 982-9. Nuytemans Karen, Bademci Guney, Inchausti Vanessa, Dressen Amy, Kinnamon Daniel D, Mehta Arpit, Wang Liyong, Züchner Stephan, Beecham Gary W, Martin Eden R, Scott William K, Vance Jeffery |
Disease penetrance of late-onset parkinsonism: a meta-analysis. JAMA neurology 2014 Dec 71 (12): 1535-9. Trinh Joanne, Guella Ilaria, Farrer Matthew Jam |
Association analysis of EIF4G1 and Parkinson disease in Xinjiang Uygur and Han nationality. Medicine 2018 May 97 (18): e0234. Ma Yu, Zheng Daxiong, Li Hongy |
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- Page last updated:May 06, 2024
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