Recognition, diagnosis and treatment of homozygous familial hypercholesterolemia
Author:
Affiliation:
1. Departments of Medicine, Division of Translational Medicine & Human Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA
Funder
NIHNHLBI
Publisher
Informa UK Limited
Subject
Pharmacology (medical),Health Policy,Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
Link
https://www.tandfonline.com/doi/pdf/10.1080/21678707.2017.1394841
Reference91 articles.
1. Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: Consensus Statement of the European Atherosclerosis Society
2. Homozygous autosomal dominant hypercholesterolaemia in the Netherlands: prevalence, genotype–phenotype relationship, and clinical outcome
3. Homozygous familial hypercholesterolemia: Current perspectives on diagnosis and treatment
4. Mechanisms of Disease: genetic causes of familial hypercholesterolemia
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