A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

Author:

Sharma Manu,Ioannidis John P A,Aasly Jan O,Annesi Grazia,Brice Alexis,Bertram Lars,Bozi Maria,Barcikowska Maria,Crosiers David,Clarke Carl E,Facheris Maurizio F,Farrer Matthew,Garraux Gaetan,Gispert Suzana,Auburger Georg,Vilariño-Güell Carles,Hadjigeorgiou Georgios M,Hicks Andrew A,Hattori Nobutaka,Jeon Beom S,Jamrozik Zygmunt,Krygowska-Wajs Anna,Lesage Suzanne,Lill Christina M,Lin Juei-Jueng,Lynch Timothy,Lichtner Peter,Lang Anthony E,Libioulle Cecile,Murata Miho,Mok Vincent,Jasinska-Myga Barbara,Mellick George D,Morrison Karen E,Meitnger Thomas,Zimprich Alexander,Opala Grzegorz,Pramstaller Peter P,Pichler Irene,Park Sung Sup,Quattrone Aldo,Rogaeva Ekaterina,Ross Owen A.,Stefanis Leonidas,Stockton Joanne D,Satake Wataru,Silburn Peter A,Strom Tim M,Theuns Jessie,Tan Eng- King,Toda Tatsushi,Tomiyama Hiroyuki,Uitti Ryan J,Van Broeckhoven Christine,Wirdefeldt Karin,Wszolek Zbigniew,Xiromerisiou Georgia,Yomono Harumi S,Yueh Kuo-Chu,Zhao Yi,Gasser Thomas,Maraganore Demetrius,Krüger Rejko,

Publisher

BMJ

Subject

Genetics (clinical),Genetics

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