Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).
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| Title: | Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2). |
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| Authors: | Lange LM; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany., Avenali M; IRCCS Mondino Foundation, Pavia, Italy.; Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy., Ellis M; Northcott Neuroscience Laboratory, ANZAC Research Institute, Concord, NSW, Australia.; Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia., Illarionova A; German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany., Keller Sarmiento IJ; Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA., Tan AH; Division of Neurology, Department of Medicine, and the Mah Pooi Soo and Tan Chin Nam Centre for Parkinson's and Related Disorders, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia., Madoev H; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany., Galandra C; IRCCS Mondino Foundation, Pavia, Italy.; Department of Molecular Medicine, University of Pavia, Pavia, Italy., Junker J; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany., Roopnarain K; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany., Solle J; Department of Clinical Research, Michael J. Fox Foundation for Parkinson's Research, New York City, NY, USA., Wegel C; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, USA., Fang ZH; German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany., Heutink P; German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany., Kumar KR; Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.; Molecular Medicine Laboratory and Neurology Department, Concord Repatriation General Hospital, The University of Sydney, Concord, NSW, Australia., Lim SY; Division of Neurology, Department of Medicine, and the Mah Pooi Soo and Tan Chin Nam Centre for Parkinson's and Related Disorders, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia., Valente EM; IRCCS Mondino Foundation, Pavia, Italy.; Department of Molecular Medicine, University of Pavia, Pavia, Italy., Nalls M; Data Tecnica International, Washington, DC, USA.; Center for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.; Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA., Blauwendraat C; Center for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.; Integrative Genomics Unit, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA., Singleton A; Center for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.; Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA., Mencacci N; Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA., Lohmann K; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany., Klein C; Institute of Neurogenetics, University of Lübeck, Lübeck, Germany. christine.klein@neuro.uni-luebeck.de. |
| Corporate Authors: | Global Parkinson’s Genetic Program (GP2) |
| Source: | NPJ Parkinson's disease [NPJ Parkinsons Dis] 2023 Sep 13; Vol. 9 (1), pp. 133. Date of Electronic Publication: 2023 Sep 13. |
| Publication Type: | Published Erratum |
| Journal Info: | Publisher: Nature Publishing Group Country of Publication: United States NLM ID: 101675390 Publication Model: Electronic Cited Medium: Print ISSN: 2373-8057 (Print) Linking ISSN: 23738057 NLM ISO Abbreviation: NPJ Parkinsons Dis Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 2373-8057 |
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| DOI: | 10.1038/s41531-023-00560-7 |
