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; ... (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), p. 133. Nature Publishing Group 10.1038/s41531-023-00560-7
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Item Type: |
Journal Article (Further Contribution) |
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Division/Institute: |
04 Faculty of Medicine > Department of Gynaecology, Paediatrics and Endocrinology (DFKE) > Clinic of Human Genetics |
Subjects: |
600 Technology > 610 Medicine & health |
ISSN: |
2373-8057 |
Publisher: |
Nature Publishing Group |
Language: |
English |
Submitter: |
André Schaller |
Date Deposited: |
04 Jan 2024 11:59 |
Last Modified: |
04 Jan 2024 12:07 |
Publisher DOI: |
10.1038/s41531-023-00560-7 |
PubMed ID: |
37704671 |
Additional Information: |
Christiane Zweier is part of the Collaborators: Global Parkinson’s Genetic Program (GP2) |
BORIS DOI: |
10.48350/189661 |
URI: |
https://boris.unibe.ch/id/eprint/189661 |
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