Lack of association of the prothrombin gene variant G20210A with myocardial infarction in Caucasian males.

Coulet, F

Lack of association of the prothrombin gene variant G20210A with myocardial infarction in Caucasian males. [electronic resource] - Thrombosis and haemostasis May 2000 - 796-7 p. digital

Publication Type: Letter; Multicenter Study

0340-6245


3' Untranslated Regions--genetics
Adult
Alleles
DNA Mutational Analysis
Europe--epidemiology
Gene Frequency
Genetic Predisposition to Disease
Humans
Male
Middle Aged
Myocardial Infarction--epidemiology
Prothrombin--genetics
Risk Factors
White People--genetics