Bibliographic Details
| Title: |
Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) |
| Authors: |
Lange, LM, Avenali, M, Ellis, M, Illarionova, A, Keller Sarmiento, IJ, Tan, A-H, Madoev, H, Galandra, C, Junker, J, Roopnarain, K, Solle, J, Wegel, C, Fang, Z-H, Heutink, P, Kumar, KR, Lim, S-Y, 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, J-C, Westenberger, A, Mollenhauer, B, Vollstedt, E-J, 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, GH-F, Ip, N, Cheung, NY-F, Zhou, X, Kishore, A, KP, D, Pal, P, Kukkle, PL, Rajan, R, Borgohain, R, Salari, M, Quattrone, A, Parnetti, L, Schirinzi, T, Funayama, M, Hattori, N, Shiraishi, T, Karimova, A, Kaishibayeva, G, Shambetova, C, Krüger, R, Tan, AH, Ahmad-Annuar, A, Norlinah, MI, Murad, NAA, Ibrahim, NM, Azmin, S, Mohamed, W, Tay, YW, Martinez-Ramirez, D, Rodriguez-Violante, M, Reyes-Pérez, P, Tserensodnom, B, Ojha, R, Anderson, TJ, Pitcher, TL, Sanyaolu, A, Okubadejo, N, Ojo, O, Aasly, JO, Pihlstrøm, L, Tan, M, Ur-Rehman, S, Cornejo-Olivas, M, Doquenia, ML, Rosales, R, Vinuela, A, Iakovenko, E, Mubarak, BA, Umair, M, Tan, E-K, Foo, JN, Amod, F, Carr, J, Bardien, S, Jeon, B, Kim, YJ, Cubo, E, Alvarez, I, Hoenicka, J, Beyer, K, Periñan, MT, Pastor, P, El-Sadig, S, Zweier, C, Paul, K, Lin, C-H, Wu, H-C, Kung, P-J, Wu, R-M, Wu, S, Wu, Y, Amouri, R, Sassi, SB, Başak, AN, Genc, G, Çakmak, ÖÖ, Ertan, S, Noyce, A, Martínez-Carrasco, A, Schrag, A, Schapira, A, Carroll, C, Bale, C, Grosset, D, Stafford, EJ, Houlden, H, Morris, HR, Hardy, J, Mok, KY, Rizig, M, Wood, N, Williams, N, Okunoye, O, Lewis, PA, Kaiyrzhanov, R, Weil, R, Love, S, Stott, S, Jasaitye, S, Dey, S, Obese, V, Espay, A, O’Grady, A, Singleton, AB, Sobering, AK, Siddiqi, B, Casey, B, Fiske, B, Jonas, C, Cruchaga, C, Pantazis, CB, Comart, C, Vitale, D, Hall, D, Hernandez, D, Shiamim, E, Riley, E, Faghri, F, Serrano, GE, Leonard, H, Iwaki, H, Chen, H, Mata, IF, Sarmiento, IJK, Williamson, J, Kim, JJ, Jankovic, J, Shulman, J, Solle, JC, Murphy, K, Nuytemans, K, Kieburtz, K, Markopoulou, K, Marek, K, Levine, KS, Chahine, LM, Screven, L, Ruffrage, L, Shulman, L, Marsili, L, Kuhl, M, Dean, M, Makarious, MB, Koretsky, M, Inca-Martinez, M, Nalls, MA, Louie, N, Mencacci, NE, Albin, R, Alcalay, R, Walker, R, Bandres-Ciga, S, Chowdhury, S, Dumanis, S, Lubbe, S, Xie, T, Foroud, T, Beach, T, Sherer, T, Song, Y, Nguyen, D, Nguyen, T, Atadzhanov, M |
| Publisher Information: |
Springer Science and Business Media LLC United States |
| Publication Year: |
2023 |
| Collection: |
PEARL (Plymouth Electronic Archiv & ResearchLibrary, Plymouth University) |
| Subject Terms: |
Global Parkinson’s Genetic Program (GP2) |
| Description: |
Correction to: s41531-023-00526-9 npj Parkinson’s Disease, published online 27 June 2023 In this article the Global Parkinson’s Genetics Program (GP2) members names and affiliations were missing in the main author list of the Original article which are listed in the below. |
| Document Type: |
article in journal/newspaper |
| File Description: |
133-; Electronic; application/pdf |
| Language: |
English |
| ISSN: |
2373-8057 |
| Relation: |
E-ISSN:2373-8057; 133; https://pearl.plymouth.ac.uk/handle/10026.1/21803 |
| DOI: |
10.1038/s41531-023-00560-7 |
| Availability: |
https://pearl.plymouth.ac.uk/handle/10026.1/21803 https://doi.org/10.1038/s41531-023-00560-7 |
| Accession Number: |
edsbas.C394B5C8 |
| Database: |
BASE |