Non-cholesterol sterols, absorption and synthesis of cholesterol and apolipoprotein A-I kinetics in a Finnish lecithin-cholesterol acyltransferase deficient family
- 1 July 1992
- journal article
- Published by Elsevier in Atherosclerosis
- Vol. 95 (1) , 25-33
- https://doi.org/10.1016/0021-9150(92)90172-d
Abstract
No abstract availableKeywords
This publication has 40 references indexed in Scilit:
- 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
- Plasma lipoprotein abnormalities in heterozygotes for familial lecithin:cholesterol acyltransferase deficiencyMetabolism, 1988
- Distribution of lecithin-cholesterol acyltransferase (LCAT) in human plasma lipoprotein fractions. Evidence for the association of active LCAT with low density lipoproteinsBiochemical and Biophysical Research Communications, 1982
- Familial lecithin-cholesterol acyltransferase deficiency in a Japanese family: Evidence for functionally defective enzyme in homozygotes and obligate heterozygotesHuman Genetics, 1982
- Familial lecithin-cholesterol acyltransferase: Identification of heterozygotes with half-normal enzyme activity and massHuman Genetics, 1981
- Familial Lecithin‐Cholesterol Acyltransferase Deficiency in Four Norwegian FamiliesActa Medica Scandinavica, 1981
- Familial Lecithin:Cholesterol Acyltransferase DeficiencyActa Medica Scandinavica, 1981
- Plasma Lipoproteins in Familial Lecithin:Cholesterol Acyltransferase Deficiency FURTHER STUDIES OF VERY LOW AND LOW DENSITY LIPOPROTEIN ABNORMALITIESJournal of Clinical Investigation, 1973
- FAMILIAL SERUM CHOLESTEROL ESTER DEFICIENCYActa Medica Scandinavica, 1968
- Familial Plasma Lecithin: Cholesterol Acyltransferase Deficiency Biochemical Study of a New Inborn Error of MetabolismScandinavian Journal of Clinical and Laboratory Investigation, 1967