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pubmed-article:10785872pubmed:abstractTextIron is suspected to play a role in the development of atherosclerosis and in the progression of the disease, and consequently in myocardial infarction. Authors of a recent study identified a mutation in HLA-H gene, C282Y, that is an excellent marker for hemochromatosis, which is the most common cause of iron overload. There is a high prevalence of carriers of heterozygous hemochromatosis, most of whom are asymptomatic even with abnormalities of iron metabolism.lld:pubmed
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pubmed-article:10785872pubmed:articleTitleC282Y mutation in the HLA-H gene is not a risk factor for patients with myocardial infarction.lld:pubmed
pubmed-article:10785872pubmed:affiliationHemocentro da Unicamp, FCM Campinas, São Paulo, Brazil. joyce@obelix.unicamp.brlld:pubmed
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