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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 23, 2025. (Total: 235602Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Parkinson Disease and PARK7[original query]
Detection of Parkin (PARK2) and DJ1 (PARK7) mutations in early-onset Parkinson disease: Parkin mutation frequency depends on ethnic origin of patients.
Human mutation 2004 May 23 (5): 525.
Djarmati A, Hedrich K, Svetel M, Schäfer N, Juric V, Vukosavic S, Hering R, Riess O, Romac S, Klein C, Kostic V
DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease.
Neurology 2004 Feb 62 (3): 389-94.
Hedrich K, Djarmati A, Schäfer N, Hering R, Wellenbrock C, Weiss P H, Hilker R, Vieregge P, Ozelius L J, Heutink P, Bonifati V, Schwinger E, Lang A E, Noth J, Bressman S B, Pramstaller P P, Riess O, Klein
Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population.
Human mutation 2009 Jul 30 (7): 1054-61.
Nuytemans Karen, Meeus Bram, Crosiers David, Brouwers Nathalie, Goossens Dirk, Engelborghs Sebastiaan, Pals Philippe, Pickut Barbara, Van den Broeck Marleen, Corsmit Ellen, Cras Patrick, De Deyn Peter P, Del-Favero Jurgen, Van Broeckhoven Christine, Theuns Jess
Incidence of mutations in the PARK2, PINK1, PARK7 genes in Polish early-onset Parkinson disease patients.
Neurologia i neurochirurgia polska 0 47 (4): 319-24.
Koziorowski D, Hoffman-Zacharska D, S?awek J, Jamrozik Z, Janik P, Potulska-Chromik A, Roszmann A, Tataj R, Bal J, Friedman
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