Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)

Lara M. Lange, Micol Avenali, Melina Ellis, Anastasia Illarionova, Sarmiento IJ Keller, Ai Huey Tan, Harutyun Madoev, Caterina Galandra, Johanna Junker, Karisha Roopnarain, Justin Solle, Claire Wegel, Zih Hua Fang, Peter Heutink, Kishore R. Kumar, Shen Yang Lim, Enza Maria Valente, Mike Nalls, Cornelis Blauwendraat, Andrew SingletonNiccolo Mencacci, Katja Lohmann, Christine Klein*, Emilia M. Gatto, Marcelo Kauffman, Samson Khachatryan, Zaruhi Tavadyan, Claire E. Shepherd, Julie Hunter, Kishore R. Kumar, Melina Ellis, Miguel E. Rentería, Sulev Koks, Alexander Zimprich, Artur F. Schumacher-Schuh, Carlos Rieder, Paula Saffie Awad, Vitor Tumas, Sarah Camargos, EA Fon, Oury Monchi, T Fon, Benjamin Pizarro Galleguillos, Marcelo Miranda, Maria Leonor Bustamante, Patricio Olguin, Pedro Chana, Beisha Tang, Huifang Shang, Jifeng Guo, Piu Chan, W Luo, G Arboleda, J Orozco, Rio MJ del, A Hernandez, M Salama, WA Kamel, YZ Zewde, A Brice, J-C Corvol, A Westenberger, Anastasia Illarionova, B Mollenhauer, Christine Klein*, E-J Vollstedt, F Hopfner, G Höglinger, Harutyun Madoev, J Trinh, Johanna Junker, Katja Lohmann, Lara M. Lange, M Sharma, S Groppa, T Gasser, Zih Hua Fang, A Akpalu, G Xiromerisiou, G Hadjigorgiou, I Dagklis, I Tarnanas, L Stefanis, M Stamelou, E Dadiotis, A Medina, Piu Chan, N Ip, NY-F Cheung, Piu Chan, Camille Carroll

*Corresponding author for this work

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