학술논문
Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)
Document Type
Article
Author
Lange, L.M.; Madoev, H.; Junker, J.; Roopnarain, K.; Lohmann, K.; Klein, C.; Avenali, M.; Galandra, C.; Valente, E.M.; Ellis, M.; Illarionova, A.; Fang, Z.-H.; Heutink, P.; Keller Sarmiento, I.J.; Mencacci, N.; Tan, A.-H.; Lim, S.-Y.; Solle, J.; Wegel, C.; Kumar, K.R.; Nalls, M.; Blauwendraat, C.; Singleton, A.
Source
In: npj Parkinson's Disease . (npj Parkinson's Disease, December 2023, 9(1))
Subject
Language
English
ISSN
23738057