Impact of statin therapy on LDL and non-HDL cholesterol levels in subjects with heterozygous familial hypercholesterolaemia
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine,Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism,Medicine (miscellaneous)
Reference34 articles.
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2. Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia;Innerarity;J Lipid Res,1990
3. Mutations and polymorphisms in the proprotein convertase subtilisin/kexin 9 (PCSK9) gene in cholesterol metabolism and disease;Abifadel;Hum Mutat,2009
4. The p.Leu167del mutation in APOE gene causes autosomal dominant hypercholesterolemia by down-regulation of LDL receptor expression in hepatocytes;Cenarro;J Clin Endocrinol Metab,2016
5. Coronary artery disease in 116 kindred with familial type II hyperlipoproteinemia;Stone;Circulation,1974
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