Genetic lipid disorders in cardiovascular disease
- 1 July 1992
- journal article
- review article
- Published by Elsevier in Trends in Cardiovascular Medicine
- Vol. 2 (4) , 140-145
- https://doi.org/10.1016/1050-1738(92)90021-j
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Familial lipoprotein disorders in patients with premature coronary artery disease.Circulation, 1992
- Lipoprotein cholesterol, apolipoprotein A-I and B and lipoprotein (a) abnormalities in men with premature coronary artery diseaseJournal of the American College of Cardiology, 1992
- Prevalence of lipoprotein (a) [Lp(a)] excess in coronary artery diseaseThe American Journal of Cardiology, 1991
- A frameshift mutation in the human apolipoprotein A-I gene causes high density lipoprotein deficiency, partial lecithin: cholesterol-acyltransferase deficiency, and corneal opacities.Journal of Clinical Investigation, 1991
- THE LDL RECEPTOR LOCUS IN FAMILIAL HYPERCHOLESTEROLEMIA: Mutational Analysis of a Membrane ProteinAnnual Review of Genetics, 1990
- DNA polymorphisms of the apolipoprotein B gene in patients with premature coronary artery diseaseAtherosclerosis, 1990
- Evidence for a dominant gene that suppresses hypercholesterolemia in a family with defective low density lipoprotein receptors.Journal of Clinical Investigation, 1989
- Detection and characterization of the heterozygote state for lipoprotein lipase deficiency.Arteriosclerosis: An Official Journal of the American Heart Association, Inc., 1989
- Apolipoprotein E polymorphism and atherosclerosis.Arteriosclerosis: An Official Journal of the American Heart Association, Inc., 1988
- A Receptor-Mediated Pathway for Cholesterol HomeostasisScience, 1986