N-acetyltransferase 2 polymorphism in Parkinson's disease. The Rotterdam study

The N-acetyltransferase-2 gene (NAT-2) has been associated with Parkinson's disease. The genotype associated with slow acetylation has been reported to be increased in patients with Parkinson's disease. Three mutant alleles M1, M2, and M3 of NAT-2 were investigated in 80 patients with idiopathic Parkinson's disease and 161 age matched randomly selected controls from a prospective population based cohort study. The allelic frequencies and genotypic distributions in patients were very similar to those found in controls. In controls the frequency of the wild type allele increased significantly wi... Mehr ...

Verfasser: Harhangi, B.S. (Biswadjiet)
Oostra, B.A. (Ben)
Heutink, P. (Peter)
Duijn, C.M. (Cornelia) van
Hofman, A. (Albert)
Breteler, M.M.B. (Monique)
Dokumenttyp: Artikel
Erscheinungsdatum: 1999
Schlagwörter: Aged / 80 and over / Arylamine N-Acetyltransferase/*genetics / EC 2.3.1.5 (Arylamine N-Acetyltransferase) / EC 2.3.1.87 (arylalkylamine-N-acetyltransferase) / Female / Frontal lobe dementia / Genotype / Human / Male / Middle Aged / Netherlands / Parkinson Disease/*genetics / Polymorphism (Genetics)/*genetics / Prospective Studies / Support / Non-U.S. Gov't
Sprache: Englisch
Permalink: https://search.fid-benelux.de/Record/base-26832884
Datenquelle: BASE; Originalkatalog
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Link(s) : http://repub.eur.nl/pub/5896