Podrobná bibliografia
| Názov: |
Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) |
| Autori: |
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 |
| Informácie o vydavateľovi: |
Springer Science and Business Media LLC
United States |
| Rok vydania: |
2023 |
| Zbierka: |
PEARL (Plymouth Electronic Archiv & ResearchLibrary, Plymouth University) |
| Predmety: |
Global Parkinson’s Genetic Program (GP2) |
| Popis: |
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. |
| Druh dokumentu: |
article in journal/newspaper |
| Popis súboru: |
133-; Electronic; application/pdf |
| Jazyk: |
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 |
| Dostupnosť: |
https://pearl.plymouth.ac.uk/handle/10026.1/21803
https://doi.org/10.1038/s41531-023-00560-7 |
| Prístupové číslo: |
edsbas.C394B5C8 |
| Databáza: |
BASE |
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