Genetic Heterogeneity in Familial Lecithin:Cholesterol Acyltransferase (LCAT) Deficiency
- 12 January 1981
- journal article
- Published by Wiley in Acta Medica Scandinavica
- Vol. 210 (1-6) , 1-2
- https://doi.org/10.1111/j.0954-6820.1981.tb09766.x
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Familial Lecithin:Cholesterol Acyltransferase DeficiencyActa Medica Scandinavica, 1981
- Radioimmunoassay of human plasma lecithin-cholesterol acyltransferase.Journal of Clinical Investigation, 1981
- Familial Lecithin: Cholesterol Acyltransferase Deficiency Complicated with Unconjugated Hyperbilirubinemia and Peripheral NeuropathyActa Medica Scandinavica, 1978
- Genetics of LCAT (lecithin:cholesterol acyltransferase) deficiencyAnnals of Human Genetics, 1975
- Familial Lecithin: Cholesterol Acyltransferase Deficiency: Report of a Third Norwegian Family with Two Afflicted MembersScandinavian Journal of Clinical and Laboratory Investigation, 1974
- FAMILIAL LCAT DEFICIENCYActa Medica Scandinavica, 1973
- Familial Plasma Lecithin:Cholesterol Acyltransferase DeficiencyBMJ, 1969
- 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