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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
Towns, Clodagh; Richer, Madeleine; Jasaityte, Simona; Stafford, Eleanor J; Joubert, Julie; Antar, Tarek; Martinez-Carrasco, Alejandro; Makarious, Mary B; Casey, Bradford; Vitale, Dan; Levine, Kristin; Leonard, Hampton; Pantazis, Caroline B; Screven, Laurel A; Hernandez, Dena G; Wegel, Claire E; Solle, Justin; Nalls, Mike A; Blauwendraat, Cornelis; Singleton, Andrew B; ... (2023). Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2). NPJ Parkinson's disease, 9(1), p. 131. Nature Publishing Group 10.1038/s41531-023-00533-w
