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RAB32 Variants in a German Parkinson's Disease Cohort.
Gabbert C, Shambetova C, Much C, Trinh J, Klein C. Gabbert C, et al. Among authors: trinh j. Mov Disord. 2024 Nov;39(11):2121-2123. doi: 10.1002/mds.30005. Epub 2024 Sep 19. Mov Disord. 2024. PMID: 39297534 No abstract available.
Team Science Approaches to Unravel Monogenic Parkinson's Disease on a Global Scale.
Junker J, Lange LM, Vollstedt EJ, Roopnarain K, Doquenia MLM, Annuar AA, Avenali M, Bardien S, Bahr N, Ellis M, Galandra C, Gasser T, Heutink P, Illarionova A, Kanana Y, Keller Sarmiento IJ, Kumar KR, Lim SY, Madoev H, Mata IF, Mencacci NE, Nalls MA, Padmanabhan S, Shambetova C, Solle JC, Tan AH, Trinh J, Valente EM, Singleton A, Blauwendraat C, Lohmann K, Fang ZH, Klein C; Global Parkinson's Genetics Program (GP2). Junker J, et al. Among authors: trinh j. Mov Disord. 2024 Oct;39(10):1868-1873. doi: 10.1002/mds.29925. Epub 2024 Jul 30. Mov Disord. 2024. PMID: 39076159
202 results