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Understanding monogenic Parkinson's disease at 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 J, 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: lohmann k. medRxiv [Preprint]. 2024 Apr 9:2024.03.12.24304154. doi: 10.1101/2024.03.12.24304154. medRxiv. 2024. PMID: 38529492 Free PMC article. Preprint.
Mutations in VPS26A are not a frequent cause of Parkinson's disease.
Koschmidder E, Mollenhauer B, Kasten M, Klein C, Lohmann K. Koschmidder E, et al. Among authors: lohmann k. Neurobiol Aging. 2014 Jun;35(6):1512.e1-2. doi: 10.1016/j.neurobiolaging.2013.12.016. Epub 2013 Dec 27. Neurobiol Aging. 2014. PMID: 24417787
The many faces of TUBB4A mutations.
Lohmann K, Klein C. Lohmann K, et al. Neurogenetics. 2014 May;15(2):81-2. doi: 10.1007/s10048-014-0399-8. Epub 2014 Mar 21. Neurogenetics. 2014. PMID: 24652610 No abstract available.
434 results