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The mutation Ala677-->Val in the methylene tetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis.
Mild hyperhomocysteinemia has been identified as a risk factor for arterial disease and for venous thrombosis. Individuals homozygous for the thermolabile variant of the methylene tetrahydrofolateExpand
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Prevalence of the prothrombin gene variant 20210 G --> A among patients with myocardial infarction.
OBJECTIVE The aim of this study was to determine the prevalence of the prothrombin variant allele 20210A among survivors of myocardial infarction. BACKGROUND The prothrombin gene variant has beenExpand
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C282Y mutation in the HLA-H Gene is Not a Risk Factor for Patients with Myocardial Infarction
TLDR
We identified a mutation in HLA-H gene, C282Y, that is an excellent marker for hemochromatosis, which is the most common cause of iron overload. Expand
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