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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 9, 2023. (Total: 217765Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Parkinson Disease and ATP13A2[original query]
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
Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore.
Neurology 2008 Nov 71 (21): 1727-32.
Lin C H, Tan E K, Chen M L, Tan L C, Lim H Q, Chen G S, Wu R
Genetic basis of Parkinson disease.
Neurosurgical focus 2010 1 28 (1): E7.
Xiromerisiou Georgia, Dardiotis Efthimios, Tsimourtou Vaïa, Kountra Persa Maria, Paterakis Konstantinos N, Kapsalaki Eftychia Z, Fountas Kostas N, Hadjigeorgiou Georgios
High-resolution arrays reveal burden of copy number variations on Parkinson disease genes associated with increased disease risk in random cohorts.
Neurological research 2016 Jul 1-11.
Murthy Megha N, Veerappa Avinash M, Seshachalam Keshava B, Ramachandra Nallur
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