Lack of association between factor V Leiden and prothrombin G20210A polymorphisms in Tunisian subjects with a history of myocardial infarction

Abstract Background Myocardial infarction is a multifactorial disease. It is provoked by occlusions in the coronary arteries resulting from exposure to multiple risk factors. Objective To study the risk of myocardial infarction associated with the gene polymorphisms of factor V Leiden and factor II...

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Veröffentlicht in:	Cardiovascular pathology 2013, Vol.22 (1), p.39-41
Hauptverfasser:	Berredjeb Ben Slama, Dhouha, Fekih-Mrissa, Najiba, Haggui, Abdeddayem, Nsiri, Brahim, Baraket, Nadia, Haouala, Habib, Gritli, Nasreddine
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Case-Control Studies DNA Mutational Analysis Factor V - genetics Factor V Leiden FII G20210A Gene Frequency Genetic Predisposition to Disease Hospitals, Military Humans Middle Aged Mutation Myocardial infarction Myocardial Infarction - genetics Odds Ratio Pathology Phenotype Polymorphism, Genetic Prothrombin - genetics Risk Factors Tunisia Young Adult
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