Elevated PCSK9 Levels in Untreated Patients With Heterozygous or Homozygous Familial Hypercholesterolemia and the Response to High‐Dose Statin Therapy
Author:
Affiliation:
1. Carbohydrate and Lipid Metabolism Research Unit, Department of Medicine, University of the Witwatersrand, Johannesburg, South Africa
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Cardiology and Cardiovascular Medicine
Reference32 articles.
1. Update and Analysis of the University College London Low Density Lipoprotein Receptor Familial Hypercholesterolemia Database
2. Homozygous familial hypercholesterolemia: Current perspectives on diagnosis and treatment
3. Genetic defects causing familial hypercholesterolaemia: Identification of deletions and duplications in the LDL-receptor gene and summary of all mutations found in patients attending the Hammersmith Hospital Lipid Clinic
4. Mutations in PCSK9 cause autosomal dominant hypercholesterolemia
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