Coulet, F <br/><br/>
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 
<br/><br/> Publication Type: Letter; Multicenter Study 
<br/><br/><label>ISSN: </label>0340-6245 
<br/><br/><label>Subjects--Topical Terms: </label><br/>3' Untranslated Regions--genetics<br/>Adult<br/>Alleles<br/>DNA Mutational Analysis<br/>Europe--epidemiology<br/>Gene Frequency<br/>Genetic Predisposition to Disease<br/>Humans<br/>Male<br/>Middle Aged<br/>Myocardial Infarction--epidemiology<br/>Prothrombin--genetics<br/>Risk Factors<br/>White People--genetics