Author:
Martinez-Hervas Sergio,Ascaso Juan F.
Reference30 articles.
1. Genetic causes of monogenic heterozygous familial hypercholesterolemia: a HuGE prevalence review;Austin;American Journal of Epidemiology,2004
2. A new PCSK9 gene promoter variant affects gene expression and causes autosomal dominant hypercholesterolemia;Blesa;Journal of Clinical Endocrinology and Metabolism,2008
3. Familial hypercholesterolemia;Bouhairie;Endocrinology and Metabolism Clinics of North America,2016
4. Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease risk;Calandra;Journal of Lipid Research,2011
5. Catapano, A.L., Graham, I., De Backer, G., et al. The Task Force for the management of dyslipidaemias of the European Society of Cardiology (ESC) and the European Atherosclerosis Society (EAS). (2016) ESC/EAS guidelines for the management of dyslipidaemias. Atherosclerosis 253, 281–344.
Cited by
8 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献