Genetics of LCAT (lecithin:cholesterol acyltransferase) deficiency
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-1809.1975.tb00617.x/fullpdf
Reference21 articles.
1. Plasma lipoproteins in familial lecithin: cholesterol acyltransferase deficiency: structure of low and high density lipoproteins as revealed by electron microscopy
2. Population structure in Norway Inbreeding, distance and kinship
3. Familial Lecithin: Cholesterol Acyltransferase Deficiency: Report of a Third Norwegian Family with Two Afflicted Members
4. Familial Lecithin: Cholesterol Acyltransferase Deficiency: Report of a Third Norwegian Family with Two Afflicted Members
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1. Scandinavian journal of gastroenterology – the editors-in-chief;Scandinavian Journal of Gastroenterology;2015-03-24
2. Characteristic kidney pathology, gene abnormality and treatments in LCAT deficiency;Clinical and Experimental Nephrology;2013-10-31
3. Lecithin:cholesterol acyltransferase: old friend or foe in atherosclerosis?;Journal of Lipid Research;2012-09
4. Two novel frame shift mutations in lecithin:cholesterol acyltransferase (LCAT) gene associated with a familial LCAT deficiency phenotype;Atherosclerosis;2009-10
5. Familial Plasma Lecithin: Cholesterol Acyltransferase Deficiency;Acta Medica Scandinavica;2009-04-24
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