The human prion gene M129V polymorphism is not associated with idiopathic Parkinson's disease in three distinct populations

Neuroscience Letters

Volumn 395, Issue 3, 2006, Pages 227-229

  Scholz, Sonja W ^a   Xiromerisiou, Georgia ^a,b   Fung, Hon C ^a,c,d   Eerola, Johanna ^e   Hellström, Olli ^f   Papadimitriou, Alexandros ^b   Hadjigeorgiou, Georgios M ^b   Tienari, Pentti J ^e   Fernandez, Hubert H ^g   Mandel, Ronald ^g   Okun, Michael S ^g   Gwinn Hardy, Katharina ^h   Singleton, Andrew B ^a  

^a NATIONAL INSTITUTE ON AGING   (United States)

^b UNIVERSITY OF THESSALY   (Greece)

^c CHANG GUNG UNIVERSITY COLLEGE OF MEDICINE   (Taiwan)

^d UNIVERSITY COLLEGE LONDON   (United Kingdom)

^e HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^f SEINÄJOKI CENTRAL HOSPITAL   (Finland)

^g UNIVERSITY OF FLORIDA   (United States)

^h NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

Author keywords

Creutzfeldt Jakob disease; M129V; Parkinson's disease; Prion

Indexed keywords

ADULT; AGED; ARTICLE; CONTROLLED STUDY; DISEASE PREDISPOSITION; FEMALE; GENE; GENE FREQUENCY; GENE LOCATION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; INCIDENCE; MAJOR CLINICAL STUDY; MALE; PARKINSON DISEASE; PRION DISEASE; PRION GENE; PRIORITY JOURNAL;

ADULT; AGED; AGED, 80 AND OVER; ALLELES; CODON; CREUTZFELDT-JAKOB SYNDROME; FEMALE; FINLAND; GENE FREQUENCY; GENOTYPE; GREECE; HUMANS; MALE; MIDDLE AGED; PARKINSON DISEASE; POLYMORPHISM, GENETIC; PRION DISEASES; PRIONS; UNITED STATES;

EID: 32244445920     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2005.10.081     Document Type: Article

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