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• W2072920128 abstract "Human MutationVolume 8, Issue 1 p. 79-82 Mutations in Brief Complete deficiency of plasma lecithin-cholesterol acyltransferase (LCAT) activity due to a novel homozygous mutation (Gly-30-Ser) in the LCAT gene James S. Owen, Corresponding Author James S. Owen University Department of Medicine, Royal Free Hospital School of Medicine, London NW3 2PF, UKUniversity Department of Medicine, Royal Free Hospital School of Medicine, London NW3 2PF, UKSearch for more papers by this authorHeiko Wiebusch, Heiko Wiebusch Institut für Arterioskleroseforschung an der Universität, 48149 Münster, GermanySearch for more papers by this authorPaul Cullen, Paul Cullen Institut für Arterioskleroseforschung an der Universität, 48149 Münster, GermanySearch for more papers by this authorGerald F. Watts, Gerald F. Watts University Department of Medicine, University of Western Australia, Royal Perth Hospital, Box X2213, GPO Perth, WA 6001, AustraliaSearch for more papers by this authorVera L.M. Lima, Vera L.M. Lima University Department of Medicine, Royal Free Hospital School of Medicine, London NW3 2PF, UKSearch for more papers by this authorHarald Funke, Harald Funke Institut für Arterioskleroseforschung an der Universität, 48149 Münster, GermanySearch for more papers by this authorGerd Assmann, Gerd Assmann Institut für Arterioskleroseforschung an der Universität, 48149 Münster, GermanySearch for more papers by this author James S. Owen, Corresponding Author James S. Owen University Department of Medicine, Royal Free Hospital School of Medicine, London NW3 2PF, UKUniversity Department of Medicine, Royal Free Hospital School of Medicine, London NW3 2PF, UKSearch for more papers by this authorHeiko Wiebusch, Heiko Wiebusch Institut für Arterioskleroseforschung an der Universität, 48149 Münster, GermanySearch for more papers by this authorPaul Cullen, Paul Cullen Institut für Arterioskleroseforschung an der Universität, 48149 Münster, GermanySearch for more papers by this authorGerald F. Watts, Gerald F. Watts University Department of Medicine, University of Western Australia, Royal Perth Hospital, Box X2213, GPO Perth, WA 6001, AustraliaSearch for more papers by this authorVera L.M. Lima, Vera L.M. Lima University Department of Medicine, Royal Free Hospital School of Medicine, London NW3 2PF, UKSearch for more papers by this authorHarald Funke, Harald Funke Institut für Arterioskleroseforschung an der Universität, 48149 Münster, GermanySearch for more papers by this authorGerd Assmann, Gerd Assmann Institut für Arterioskleroseforschung an der Universität, 48149 Münster, GermanySearch for more papers by this author First published: 1996 https://doi.org/10.1002/(SICI)1098-1004(1996)8:1<79::AID-HUMU13>3.0.CO;2-OCitations: 9AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Citing Literature Volume8, Issue11996Pages 79-82 RelatedInformation" @default.
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• W2072920128 title "Complete deficiency of plasma lecithin-cholesterol acyltransferase (LCAT) activity due to a novel homozygous mutation (Gly-30-Ser) in the LCAT gene" @default.
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