Defective enzyme causes lecithin-cholesterol acyltransferase deficiency in a Japanese kindred
- 1 July 1985
- journal article
- research article
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism
- Vol. 835 (2) , 253-257
- https://doi.org/10.1016/0005-2760(85)90280-2
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- A New Case of Familial LCAT DeficiencyActa Medica Scandinavica, 1983
- 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 Deficiency in Four Norwegian FamiliesActa 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
- Familial LCAT Deficiency Report of Two Patients from a Canadian Family of Italian and Swedish DescentScandinavian Journal of Clinical and Laboratory Investigation, 1978
- Société de Néphrologie, Paris, France, February 7, 1976Kidney International, 1976
- PRIMARY L.C.A.T.-DEFICIENCY DISEASEThe Lancet, 1975
- 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