Molecular genetic testing for autosomal dominant hypercholesterolemia in 29,449 Norwegian index patients and 14,230 relatives during the years 1993–2020
Trond P. Leren, Martin P. Bogsrud
Topics & Concepts
Familial hypercholesterolemiaPCSK9Apolipoprotein BGeneticsLDL receptorMutationGenetic testingCompound heterozygosityBiologyGene mutationGeneMolecular geneticsKexinMedicineLipoproteinEndocrinologyCholesterolLipoproteins and Cardiovascular HealthDiabetes, Cardiovascular Risks, and LipoproteinsAortic Thrombus and Embolism