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Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) von Lange, LM, Avenali, M, Ellis, M, Illarionova, A, Keller Sarmiento, IJ, Tan, AH, Madoev, H, Galandra, C, Junker, J, Roopnarain, K, Solle, J, Wegel, C, Fang, ZH, Heutink, P, Kumar, KR, Lim, SY, Valente, EM, Nalls, M, Blauwendraat, C, Singleton, A, Mencacci, N, Lohmann, K, Klein, C, Gatto, EM, Kauffman, M, Khachatryan, S, Tavadyan, Z, Shepherd, CE, Hunter, J, Kumar, K, Rentería, ME, Koks, S, Zimprich, A, Schumacher-Schuh, AF, Rieder, C, Awad, PS, Tumas, V, Camargos, S, Fon, EA, Monchi, O, Fon, T, Galleguillos, BP, Miranda, M, Bustamante, ML, Olguin, P, Chana, P, Tang, B, Shang, H, Guo, J, Chan, P, Luo, W, Arboleda, G, Orozco, J, del Rio, MJ, Hernandez, A, Salama, M, Kamel, WA, Zewde, YZ, Brice, A, Corvol, JC, Westenberger, A, Mollenhauer, B, Vollstedt, EJ, Hopfner, F, Höglinger, G, Trinh, J, Sharma, M, Groppa, S, Gasser, T, Akpalu, A, Xiromerisiou, G, Hadjigorgiou, G, Dagklis, I, Tarnanas, I, Stefanis, L, Stamelou, M, Dadiotis, E, Medina, A, Chan, GHF, Ip, N, Cheung, NYF, Zhou, X, Kishore, A, Kp, D, Pal, P, Kukkle, PL, Rajan, R, Borgohain, R, Salari, M, Quattrone, A
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