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

Authors

Christine Klein, University of Lübeck
Lara M. Lange, University of Lübeck
Micol Avenali, IRCCS Fondazione Istituto Neurologico Casimiro Mondino - Pavia
Melina Ellis, ANZAC Research Institute
Anastasia Illarionova, German Center for Neurodegenerative Diseases
Sarmiento IJ Keller
Ai Huey Tan, University of Malaya
Harutyun Madoev, University of Lübeck
Caterina Galandra, IRCCS Fondazione Istituto Neurologico Casimiro Mondino - Pavia
Johanna Junker, University of Lübeck
Karisha Roopnarain, University of Lübeck
Justin Solle, Michael J. Fox Foundation for Parkinson's Research
Claire Wegel, Indiana University Bloomington
Zih Hua Fang, German Center for Neurodegenerative Diseases
Peter Heutink, German Center for Neurodegenerative Diseases
Kishore R. Kumar, Garvan Institute of Medical Research
Shen Yang Lim, University of Malaya
Enza Maria Valente, IRCCS Fondazione Istituto Neurologico Casimiro Mondino - Pavia
Mike Nalls, Data Tecnica International
Cornelis Blauwendraat, National Institutes of Health
Andrew Singleton, National Institutes of Health
Niccolo Mencacci, Northwestern University
Katja Lohmann, University of Lübeck
Emilia M. Gatto, Sanatorio de la Trinidad
Marcelo Kauffman, Hospital General de Agudos José María Ramos Mejía
Samson Khachatryan, Somnus Neurology Clinic
Zaruhi Tavadyan, Somnus Neurology Clinic
Claire E. Shepherd, Neuroscience Research Australia
Julie Hunter, ANZAC Research Institute
Miguel E. Rentería, Queensland Institute of Medical Research

Abstract

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.

DOI

10.1038/s41531-023-00560-7

Publication Date

2023-09-13

Publication Title

npj Parkinson's Disease

Volume

9

Issue

1

Embargo Period

2023-12-19

Recommended Citation

Klein, C., Lange, L., Avenali, M., Ellis, M., Illarionova, A., Keller, S., Tan, A., Madoev, H., Galandra, C., Junker, J., Roopnarain, K., Solle, J., Wegel, C., Fang, Z., Heutink, P., Kumar, K., Lim, S., Valente, E., Nalls, M., Blauwendraat, C., Singleton, A., Mencacci, N., Lohmann, K., Gatto, E., Kauffman, M., Khachatryan, S., Tavadyan, Z., Shepherd, C., Hunter, J., & Rentería, M. (2023) 'Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)', npj Parkinson's Disease, 9(1). Available at: 10.1038/s41531-023-00560-7" >https://doi.org/10.1038/s41531-023-00560-7