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Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease

Author
HUDSON, Gavin1 ; NAILS, Mike2 ; HARDY, John6 ; WOOD, Nicholas E6 ; BURN, David J7 ; CHINNERY, Patrick F1 ; EVANS, Jonathan R3 ; BREEN, David P3 ; WINDER-RHODES, Sophie3 ; MORRISON, Karen E4 ; MORRIS, Huw R5 ; WILLIAMS-GRAY, Caroline H3 ; BARKER, Roger A4 ; SINGLETON, Andrew B2
[1] Wellcome Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom
[2] Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, United States
[3] Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom
[4] Division of Neurosciences, University of Birmingham, Edgbaston, Birmingham, United Kingdom
[5] Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff, United Kingdom
[6] Department of Molecular Neuroscience, Institute of Neurology, University College London, London, United Kingdom
[7] Institute for Ageing and Health, Newcastle University, Newcastle upon Tyne, United Kingdom
Source

Neurology. 2013, Vol 80, Num 22, pp 2042-2048, 7 p ; ref : 30 ref

CODEN
NEURAI
ISSN
0028-3878
Scientific domain
Cognition; Neurology
Publisher
Lippincott Williams & Wilkins, Hagerstown, MD
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Cytopathie mitochondriale DNA mitochondrial Maladie de Parkinson Pathologie du système nerveux Maladie mitochondriale Enzymopathie Maladie dégénérative Maladie héréditaire Maladie métabolique Pathologie de l'encéphale Pathologie du système nerveux central Syndrome extrapyramidal
Keyword (en)
Mitochondrial disorder Mitochondrial DNA Parkinson disease Nervous system diseases Enzymopathy Degenerative disease Genetic disease Metabolic diseases Cerebral disorder Central nervous system disease Extrapyramidal syndrome
Keyword (es)
Citopatía mitocondrial DNA mitocondrial Parkinson enfermedad Sistema nervioso patología Enzimopatía Enfermedad degenerativa Enfermedad hereditaria Metabolismo patología Encéfalo patología Sistema nervosio central patología Extrapiramidal síndrome
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17G Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases

Discipline
Neurology
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
27579712

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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