Illarionova, Anastasia

Klein, Christine

M. Lange, Lara

Mohamed, Wael Mohamed Yousef

Sarmiento, Ignacio J. Keller

Tan, Ai-Huey

The International Islamic University Malaysia Repository

9/21/23, 10:37 AM Scopus - Print Documenthttps://www.scopus.com/citation/print.uri?origin=recordpage&sid=&src=s&stateKey=OFD_1691687208&eid=2-s2.0-85168458606&sort=&clickedLink=&view=SpecifyFields&selectedCitationInformationItemsAll=on&se… 1/2DocumentsLange, L.M.a , Avenali, M.b c , Ellis, M.d e , Illarionova, A.f , Keller Sarmiento, I.J.g , Tan, A.-H.h , Madoev, H.a , Galandra, C.b i , Junker, J.a , Roopnarain, K.a , Solle, J.j , Wegel,C.k , Fang, Z.-H.f , Heutink, P.f , Kumar, K.R.l m , Lim, S.-Y.h , Valente, E.M.b i , Nalls, M.n o p , Blauwendraat, C.o q , Singleton, A.o p , Mencacci, N.g , Lohmann, K.a , Klein, C.a ,the Global Parkinson's Genetic Program (GP2)rElucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)(2023) npj Parkinson's Disease, 9 (1), art. no. 100, . DOI: 10.1038/s41531-023-00526-9a Institute of Neurogenetics, University of Lübeck, Lübeck, Germanyb IRCCS Mondino Foundation, Pavia, Italyc Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italyd Northcott Neuroscience Laboratory, ANZAC Research Institute, Concord, NSW, Australiae Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australiaf German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germanyg Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL, United Statesh Division of Neurology, Department of Medicine, and the Mah Pooi Soo and Tan Chin Nam Centre for Parkinson’s and Related Disorders, Faculty of Medicine, University ofMalaya, Kuala Lumpur, Malaysiai Department of Molecular Medicine, University of Pavia, Pavia, Italyj Department of Clinical Research, Michael J. Fox Foundation for Parkinson’s Research, New York City, NY, United Statesk Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, United Statesl Garvan Institute of Medical Research, Darlinghurst, NSW, Australiam Molecular Medicine Laboratory and Neurology Department, Concord Repatriation General Hospital, The University of Sydney, Concord, NSW, Australian Data Tecnica International, Washington, DC, United Stateso Center for Alzheimer’s and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health,Bethesda, MD, United Statesp Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, United Statesq Integrative Genomics Unit, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, United StatesCorrespondence AddressKlein C.; Institute of Neurogenetics, Germany; email: christine.klein@neuro.uni-luebeck.dePublisher: Nature ResearchISSN: 237380579/21/23, 10:37 AM Scopus - Print Documenthttps://www.scopus.com/citation/print.uri?origin=recordpage&sid=&src=s&stateKey=OFD_1691687208&eid=2-s2.0-85168458606&sort=&clickedLink=&view=SpecifyFields&selectedCitationInformationItemsAll=on&se… 2/2Language of Original Document: EnglishAbbreviated Source Title: NPJ Parkinson's Dis.2-s2.0-85168458606Document Type: ArticlePublication Stage: FinalSource: ScopusCopyright © 2023 Elsevier B.V. All rights reserved. Scopus® is a registered trademark of Elsevier B.V.

Author correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)

http://irep.iium.edu.my/106872/7/106872_%20Elucidating%20causative%20gene%20variants%20in%20hereditary%20Parkinson%E2%80%99s%20disease%20in%20the%20Global%20Parkinson%E2%80%99s%20Genetics%20Program_Scopus.pdf

Author correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)

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