Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).
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BORIS DOI
Publisher DOI
PubMed ID
37704671
Date of Publication
2023-09-13
Publication Type
Article
Subject(s)
Language(s)
en
Contributor(s)
Lange, Lara M | |
Avenali, Micol | |
Ellis, Melina | |
Illarionova, Anastasia | |
Keller Sarmiento, Ignacio J | |
Tan, Ai-Huey | |
Madoev, Harutyun | |
Galandra, Caterina | |
Junker, Johanna | |
Roopnarain, Karisha | |
Solle, Justin | |
Wegel, Claire | |
Fang, Zih-Hua | |
Heutink, Peter | |
Kumar, Kishore R | |
Lim, Shen-Yang | |
Valente, Enza Maria | |
Nalls, Mike | |
Blauwendraat, Cornelis | |
Singleton, Andrew | |
Mencacci, Niccolo | |
Lohmann, Katja | |
Klein, Christine |
Series
NPJ Parkinson's disease
Publisher
Nature Publishing Group
ISSN
2373-8057
Access(Rights)
open.access