Deficiency of lecithin: cholesterol acyltransferase due to compound heterozygosity of two novel mutations (Gly33Arg and 30 bp ins) in the LCAT gene

Journal Article Deficiency of lecithin: cholesterol acyltransferase due to compound heterozygosity of two novel mutations (Gly33Arg and 30 bp ins) in the LCAT gene Get access Heiko Wlebusch, Heiko Wlebusch Search for other works by this author on: Oxford Academic PubMed Google Scholar paul Cullen, paul Cullen * *To whom correspondence should be addressed Search for other works by this author on: Oxford Academic PubMed Google Scholar James S.Owen, James S.Owen 1Department of Clinical Chemistry Search for other works by this author on: Oxford Academic PubMed Google Scholar David Collins, David Collins 2Department of Endocrinology, Northwick Park Hospital, Watford Road, Harrow, Middlesex HA1 3UJUK Search for other works by this author on: Oxford Academic PubMed Google Scholar Patrick S.Sharp, Patrick S.Sharp 2Department of Endocrinology, Northwick Park Hospital, Watford Road, Harrow, Middlesex HA1 3UJUK Search for other works by this author on: Oxford Academic PubMed Google Scholar Harald Funke, Harald Funke Search for other works by this author on: Oxford Academic PubMed Google Scholar Gerd Assmann Gerd Assmann Search for other works by this author on: Oxford Academic PubMed Google Scholar Human Molecular Genetics, Volume 4, Issue 1, January 1995, Pages 143–145, https://doi.org/10.1093/hmg/4.1.143 Published: 01 January 1995 Article history Received: 11 October 1994 Accepted: 02 November 1994 Published: 01 January 1995