Homozygous hypobetalipoproteinemia with spared chylomicron formation
- 1 January 1989
- journal article
- research article
- Published by Elsevier in Metabolism
- Vol. 38 (1) , 1-7
- https://doi.org/10.1016/0026-0495(89)90172-8
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Homozygous hypobetalipoproteinemia: a disease distinct from abetalipoproproteinemia at the molecular level.Journal of Clinical Investigation, 1988
- Genetic analysis of a kindred with familial hypobetalipoproteinemia. Evidence for two separate gene defects: one associated with an abnormal apolipoprotein B species, apolipoprotein B-37; and a second associated with low plasma concentrations of apolipoprotein B-100.Journal of Clinical Investigation, 1987
- Characterization of an abnormal species of apolipoprotein B, apolipoprotein B-37, associated with familial hypobetalipoproteinemia.Journal of Clinical Investigation, 1987
- Analysis of the apolipoprotein B gene and messenger ribonucleic acid in abetalipoproteinemia.Journal of Clinical Investigation, 1986
- Apolipoprotein B: Structural and Metabolic HeterogeneityAnnual Review of Physiology, 1983
- Normotriglyceridemic abetalipoproteinemia. absence of the B-100 apolipoprotein.Journal of Clinical Investigation, 1981
- Metabolic Studies in an Unusual Case of Asymptomatic Familial Hypobetalipoproteinemia with Hypoalphalipoproteinemia and Fasting ChylomicronemiaJournal of Clinical Investigation, 1979
- Hypobetalipoproteinaemia--a variant of the Bassen-Kornzweig syndrome.Gut, 1979
- Immunochemical quantitation of antigens by single radial immunodiffusionImmunochemistry, 1965
- CONGENITAL β-LIPOPROTEIN DEFICIENCYMedicine, 1964