Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia.
Open Access
- 1 August 1990
- journal article
- review article
- Published by Elsevier in Journal of Lipid Research
- Vol. 31 (8) , 1337-1349
- https://doi.org/10.1016/s0022-2275(20)42605-7
Abstract
No abstract availableKeywords
This publication has 64 references indexed in Scilit:
- Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the formation of buoyant, triglyceride-rich lipoproteins.Journal of Clinical Investigation, 1990
- Familial Hypobetalipoproteinemia Associated with a Mutant Species of Apolipoprotein B (B-46)New England Journal of Medicine, 1989
- Lack of correlation between the apolipoprotein B Xba I polymorphism and blood lipid levels in a Swedish populationAtherosclerosis, 1989
- Cardiovascular risks: New insights from FraminghamAmerican Heart Journal, 1988
- Apolipoprotein B gene variants are involved in the determination of serum cholesterol levels: a study in normo- and hypelipidaemic individualsAtherosclerosis, 1987
- DNA Sequence of the Human Apolipoprotein B GeneDNA, 1987
- Lipoprotein Mutations in Pigs Are Associated with Elevated Plasma Cholesterol and AtherosclerosisScience, 1986
- Apolipoprotein B–Gene DNA Polymorphisms Associated with Myocardial InfarctionNew England Journal of Medicine, 1986
- Human apoB-100 gene resides in the p23 → pter region of chromosome 2Biochemical and Biophysical Research Communications, 1985
- Apolipoprotein B: Structural and Metabolic HeterogeneityAnnual Review of Physiology, 1983