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Author Correction - Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)559.61 kB
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- Title
- Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)
- Authors/Creators
- Lara M. Lange - University of LübeckMicol Avenali - University of PaviaMelina Ellis - Anzac Research InstituteAnastasia Illarionova - German Center for Neurodegenerative DiseasesIgnacio J. Keller Sarmiento - Chicago, IL USAAi-Huey Tan - University of MalayaHarutyun Madoev - University of LübeckCaterina Galandra - University of PaviaJohanna Junker - University of LübeckKarisha Roopnarain - University of LübeckJustin Solle - Michael J. Fox FoundationClaire Wegel - Indiana University – Purdue University IndianapolisZih-Hua Fang - German Center for Neurodegenerative DiseasesPeter Heutink - German Center for Neurodegenerative DiseasesKishore R. Kumar - Garvan Institute of Medical ResearchShen-Yang Lim - Kuala Lumpur, MalaysiaEnza Maria Valente - University of PaviaMike Nalls - Data Tecnica International (United States)Cornelis Blauwendraat - National Institute of Neurological Disorders and StrokeAndrew Singleton - National Institute on AgingNiccolo Mencacci - Northwestern UniversityKatja Lohmann - University of LübeckChristine Klein - University of LübeckSulev Koks - Murdoch University, Centre for Molecular Medicine and Innovative Therapeuticsthe Global Parkinson’s Genetic Program (GP2)
- Publication Details
- NPJ Parkinson's Disease, Vol.9, 133
- Publisher
- Nature Publishing Group UK
- Identifiers
- 991005606969807891
- Copyright
- © The Author(s) 2023
- Murdoch Affiliation
- Centre for Molecular Medicine and Innovative Therapeutics
- Language
- English
- Resource Type
- Journal article