Case report: A novel apolipoprotein A-I missense mutation apoA-I (Arg149Ser)Boston associated with decreased lecithin-cholesterol acyltransferase activation and cellular cholesterol efflux

Published 2015 View Full Article

Authors

Keywords

HDL deficiency, Apolipoprotein A-I, Genetic mutation, Cellular cholesterol efflux, LCAT activity, CETP activity

Journal

Journal of Clinical Lipidology

Volume 9, Issue 3, Pages 390-395

Publisher

Elsevier BV

Online

2015-03-05

DOI

10.1016/j.jacl.2015.02.005

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