Abstract
Familial hypercholesterolemia (FH) is an autosomal dominant genetic disorder characterized by very elevated LDL-c (low density lipoprotein cholesterol) plasma concentration and by increased risk of premature coronary artery disease which is caused by defects of the LDL receptor in hepatocytes and in cells such as fibroblasts that prevent the removal of LDL from the circulation. LDL partic…