| Literature DB >> 18720902 |
Géraldine Mercier1, Florent Diéterlen, Gérard Lucotte.
Abstract
Methionine homozygosity at codon 129 of the prion protein gene is a risk factor for Creutzfeldt-Jakob disease. Knowledge of M129V polymorphism in normal populations may contribute to a better understanding of prion diseases. M129V polymorphism was studied in 2201 normal subjects, originating from 15 populations from Europe and the Middle East. Mean heterozygosity in these populations is 38.9%, and there is some significant geographic heterogeneity between them. A comparison of M129 allele frequencies in these 15 populations to those already published for 8 European countries plus Turkey shows significant correlations with both latitude (r = -0.77) and longitude (r = 0.69). The geographic map of methionine allele frequencies indicates an east-west gradient of decreasing methionine allele values from the Middle East to Western Europe.Entities:
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Year: 2008 PMID: 18720902 DOI: 10.3378/1534-6617(2008)80[181:PDOTMA]2.0.CO;2
Source DB: PubMed Journal: Hum Biol ISSN: 0018-7143 Impact factor: 0.553