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Epigenetics in Familial Hypercholesterolaemia miRNA binding sites as regulators of genes involved in the lipid metabolism

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Familial hypercholesterolaemia is an autosomal dominant disorder of lipid metabolism characterized by elevated levels of LDL-C and increased cardiovascular risk. Although the disorder can be diagnosed based on established clinical criteria, only the genetic diagnosis confirms the clinical suspicion.

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Familial Hypercholesterolaemia Cholesterol Portuguese FH Study Doenças Cardio e Cérebro-vasculares

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Instituto Nacional de Saúde Doutor Ricardo Jorge, IP

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