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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)

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Titel: 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)
Autoren: Lange LM, Ellis M, Keller Sarmiento IJ, Tan A-H, Galandra C, Roopnarain K, Solle J, Fang Z-H, Heutink P, Kumar KR, Lim S-Y, Valente EM, Nalls M, Singleton A, Mencacci N, Klein C, Gatto EM, Kauffman M, Khachatryan S, Tavadyan Z, Shepherd CE, Hunter J, Kumar K, Renteria 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, Illarionova A, Mollenhauer B, Vollstedt E-J, Hopfner F, Hoglinger G, Madoev H, Trinh J, Junker J, Lohmann K, 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, Avenali M, Schirinzi T, Funayama M, Hattori N, Shiraishi T, Karimova A, Kaishibayeva G, Shambetova C, Kruger R, Ahmad-Annuar A, Norlinah MI, Murad NAA, Ibrahim NM, Azmin S, Mohamed W, Tay YW, Martinez-Ramirez D, Rodriguez-Violante M, Reyes-Perez P, Tserensodnom B, Ojha R, Anderson TJ, Pitcher TL, Sanyaolu A, Okubadejo N, Ojo O, Aasly JO, Pihlstrom 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, Perinan 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, Basak AN, Genc G, Cakmak OO, Ertan S, Noyce A, Martinez-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, Wegel C, Blauwendraat 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
Quelle: npj Parkinson's Disease, December 2023
Verlagsinformationen: Nature Research
Publikationsjahr: 2023
Bestand: Newcastle University Library ePrints Service
Beschreibung: © 2023, Springer Nature Limited.Correction to: 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.
Publikationsart: text
Sprache: unknown
Relation: https://eprints.ncl.ac.uk/296409
Verfügbarkeit: https://eprints.ncl.ac.uk/296409
Dokumentencode: edsbas.FD4C3B0
Datenbank: BASE
Beschreibung
Abstract:© 2023, Springer Nature Limited.Correction to: 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.