Complete Deficiency of Plasma Lecithin-Cholesterol Acyltransferase (LCAT) Activity Due to a Novel Homozygous Mutation (Gly-30-Ser) in the LCAT Gene

J.S. Owen, H. Wiebusch, P. Cullen, Gerald Watts, V.L.M. Lima, H. Funke, G. Assmann

Research output: Contribution to journalArticle

10 Citations (Scopus)
Original languageEnglish
Pages (from-to)79-82
JournalHuman Mutation
Issue numberN/A
Publication statusPublished - 1996

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