Lipoproteins in lecithin-cholesterol-acyltransferase (LCAT)*-deficiency
- 1 January 1975
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 27 (3) , 185-197
- https://doi.org/10.1007/bf00278345
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- On the polypeptide composition of an abnormal high density lipoprotein (LP‐E) occurring in LCAT‐deficient plasmaFEBS Letters, 1974
- An apolipoprotein preferentially enriched in cholesteryl ester-rich very low density lipoproteinsBiochemical and Biophysical Research Communications, 1974
- Identification of lipoprotein families in familial lecithin: Cholesterol acyltransferase deficiencyBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1973
- Identification of the abnormal cholestatic lipoprotein (LP‐X) in familial lecithin:Cholesterol acyltransferase deficiencyFEBS Letters, 1972
- Studies on the protein moiety of serum high density lipoprotein from patients with familial lecithin: cholesterol acyltransferase deficiencyClinical Genetics, 1972
- A protein cofactor of lecithin:Cholesterol acyltransferaseBiochemical and Biophysical Research Communications, 1972
- Purification and substrate specificity of lecithin—cholesterol acyl transferase from human plasmaFEBS Letters, 1971
- 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
- Some properties of a cholesterol esterifying enzyme in human plasmaBiochimica et Biophysica Acta (BBA) - Specialized Section on Enzymological Subjects, 1964