The genetic defect of the original Norwegian lecithin:cholesterol acyltransferase deficiency families
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/0014-5793(92)80795-I/fullpdf
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1. Human lecithin-cholesterol acyltransferase gene: complete gene sequence and sites of expression
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3. Paradoxical Esterification of Plasma Cholesterol in Fish Eye Disease
4. Evidence for Deficiency of High Density Lipoprotein Lecithin: Cholesterol Acyltransferase Activity (α-LCAT) in Fish Eye Disease
5. Evidence for the Presence in Human Plasma of Lecithin: Cholesterol Acyltransferase Activity (β-LCAT) Specifically Esterifying Free Cholesterol of Combined Pre-β- and β-Lipoproteins: Studies of Fish Eye Disease Patients and Control Subjects
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3. Novel Missense LCAT Gene Mutation Associated with an Atypical Phenotype of Familial LCAT Deficiency in Two Portuguese Brothers;JIMD Reports;2017
4. Lecithin:cholesterol acyltransferase: old friend or foe in atherosclerosis?;Journal of Lipid Research;2012-09
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