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

Lange, Lara; Avenali, Micol; Ellis, Melina; Illarionova, Anastasia J.; Sarmiento, Ignacio Keller; Tan, Ai-Huey; Madoev, Harutyun; Galandra, Caterina; Junker, Johanna; Roopnarain, Karisha; Solle, Justin; Wegel, Claire; Fang, Zih-Hua; Heutink, Peter R.; Kumar, Kishore; Lim, Shen-Yang; Valente, Enza Maria; Nalls, Mike; Blauwendraat, Cornelis; Singleton, Andrew; Mencacci, Niccolo; Lohmann, Katja; Klein, Christine

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

Author:

Lange, Lara; Avenali, Micol; Ellis, Melina; Illarionova, Anastasia J.; Sarmiento, Ignacio Keller; Tan, Ai-Huey; Madoev, Harutyun; Galandra, Caterina; Junker, Johanna; Roopnarain, Karisha; Solle, Justin; Wegel, Claire; Fang, Zih-Hua; Heutink, Peter R.; Kumar, Kishore; Lim, Shen-Yang; Valente, Enza Maria; Nalls, Mike; Blauwendraat, Cornelis; Singleton, Andrew; Mencacci, Niccolo; Lohmann, Katja; Klein, Christine

Tübinger Autor(en):

Illarionova, Anastasia
Fang, Zih-Hua
Heutink, Peter

Published in:

Npj Parkinsons Disease (2023), Bd. 9, H. 1

Verlagsangabe:

Berlin : Nature Portfolio

Language:

English

Full text:

http://dx.doi.org/10.1038/s41531-023-00526-9

ISSN:

2373-8057