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Evaluation of miR-146a (rs2910164) polymorphism in coronary artery disease: Case-control and silico analysis

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Summary: This study suggests that the C allele of the rs2910164 SNP might be under negative selection in HCM patients, and plasma levels of miR-146a-5p and GC/CC genotypes are indicative of the obstructive phenotype in HCM patients.

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