Klein HG

References (3)

Title : Fish eye syndrome: a molecular defect in the lecithin-cholesterol acyltransferase (LCAT) gene associated with normal alpha-LCAT-specific activity. Implications for classification and prognosis - Klein_1993_J.Clin.Invest_92_479
Author(s) : Klein HG , Santamarina-Fojo S , Duverger N , Clerc M , Dumon MF , Albers JJ , Marcovina S , Brewer HB, Jr.
Ref : J Clinical Investigation , 92 :479 , 1993
Abstract :
PubMedSearch : Klein_1993_J.Clin.Invest_92_479
PubMedID: 8326012

Title : Two different allelic mutations in the lecithin:cholesterol acyltransferase (LCAT) gene resulting in classic LCAT deficiency: LCAT (tyr83-->stop) and LCAT (tyr156-->asn) - Klein_1993_J.Lipid.Res_34_49
Author(s) : Klein HG , Lohse P , Duverger N , Albers JJ , Rader DJ , Zech LA , Santamarina-Fojo S , Brewer HB, Jr.
Ref : J Lipid Res , 34 :49 , 1993
Abstract :
PubMedSearch : Klein_1993_J.Lipid.Res_34_49
PubMedID: 8445342

Title : Two different allelic mutations in the lecithin-cholesterol acyltransferase gene associated with the fish eye syndrome. Lecithin-cholesterol acyltransferase (Thr123----Ile) and lecithin-cholesterol acyltransferase (Thr347----Met) - Klein_1992_J.Clin.Invest_89_499
Author(s) : Klein HG , Lohse P , Pritchard PH , Bojanovski D , Schmidt H , Brewer HB, Jr.
Ref : J Clinical Investigation , 89 :499 , 1992
Abstract :
PubMedSearch : Klein_1992_J.Clin.Invest_89_499
PubMedID: 1737840
Gene_locus related to this paper: human-LCAT