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, Ellis, M, 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
, Krüger, R & the Global Parkinson’s Genetic Program (GP2) 2023, '
Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) (npj Parkinson's Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9)',
npj Parkinson's Disease, vol. 9, no. 1, 133.
https://doi.org/10.1038/s41531-023-00560-7