Current Status of Familial LCAT Deficiency in Japan
Volume: 28, Issue: 7, Pages: 679 - 691
Published: Apr 18, 2021
Abstract
Lecithin cholesterol acyltransferase (LCAT) is a lipid-modification enzyme that catalyzes the transfer of the acyl chain from the second position of lecithin to the hydroxyl group of cholesterol (FC) on plasma lipoproteins to form cholesteryl acylester and lysolecithin. Familial LCAT deficiency is an intractable autosomal recessive disorder caused by inherited dysfunction of the LCAT enzyme. The disease appears in two different phenotypes...
Paper Details
Title
Current Status of Familial LCAT Deficiency in Japan
Published Date
Apr 18, 2021
Volume
28
Issue
7
Pages
679 - 691
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