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Investigating the Protective Role of the Mitochondrial 2158 T > C Variant in Parkinson's Disease.

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Title: Investigating the Protective Role of the Mitochondrial 2158 T > C Variant in Parkinson's Disease.
Authors: Akçimen F; Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA., van Midden V; Department of Neurology, University Medical Centre Ljubljana, Ljubljana, Slovenia., Akerman SC; Brain Science Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA., Makarious MB; Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; UCL Movement Disorders Centre, University College London, London, United Kingdom., Rothstein JD; Brain Science Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA., Fang ZH; German Center for Neurodegenerative Diseases, DZNE, Tübingen, Germany., Bandres-Ciga S; 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, Maryland, USA.
Corporate Authors: Global Parkinson's Genetics Program
Source: Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2024 Sep; Vol. 39 (9), pp. 1645-1647. Date of Electronic Publication: 2024 Jun 28.
Publication Type: Letter
Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8610688 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8257 (Electronic) Linking ISSN: 08853185 NLM ISO Abbreviation: Mov Disord Subsets: MEDLINE; In Process
Database: MEDLINE Ultimate
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  Data: Investigating the Protective Role of the Mitochondrial 2158 T > C Variant in Parkinson's Disease.
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  Data: <searchLink fieldCode="AU" term="%22Akçimen+F%22">Akçimen F</searchLink>; Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22van+Midden+V%22">van Midden V</searchLink>; Department of Neurology, University Medical Centre Ljubljana, Ljubljana, Slovenia.<br /><searchLink fieldCode="AU" term="%22Akerman+SC%22">Akerman SC</searchLink>; Brain Science Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Makarious+MB%22">Makarious MB</searchLink>; Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; UCL Movement Disorders Centre, University College London, London, United Kingdom.<br /><searchLink fieldCode="AU" term="%22Rothstein+JD%22">Rothstein JD</searchLink>; Brain Science Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.; Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Fang+ZH%22">Fang ZH</searchLink>; German Center for Neurodegenerative Diseases, DZNE, Tübingen, Germany.<br /><searchLink fieldCode="AU" term="%22Bandres-Ciga+S%22">Bandres-Ciga S</searchLink>; 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, Maryland, USA.
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              Text: 2024 Sep
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