Skretting G

References (3)

Title : An amino acid exchange in exon I of the human lecithin: cholesterol acyltransferase (LCAT) gene is associated with fish eye disease - Skretting_1992_Biochem.Biophys.Res.Commun_182_583
Author(s) : Skretting G , Prydz H
Ref : Biochemical & Biophysical Research Communications , 182 :583 , 1992
Abstract :
PubMedSearch : Skretting_1992_Biochem.Biophys.Res.Commun_182_583
PubMedID: 1571050
Gene_locus related to this paper: human-LCAT

Title : The genetic defect of the original Norwegian lecithin:cholesterol acyltransferase deficiency families. - Skretting_1992_FEBS.Lett_309_307
Author(s) : Skretting G , Blomhoff JP , Solheim J , Prydz H
Ref : FEBS Letters , 309 :307 , 1992
Abstract :
PubMedSearch : Skretting_1992_FEBS.Lett_309_307
PubMedID: 1516702
Gene_locus related to this paper: human-LCAT

Title : The isolation and characterisation of a cDNA clone for human lecithin:cholesterol acyl transferase and its use to analyse the genes in patients with LCAT deficiency and fish eye disease - Rogne_1987_Biochem.Biophys.Res.Commun_148_161
Author(s) : Rogne S , Skretting G , Larsen F , Myklebost O , Mevag B , Carlson LA , Holmquist L , Gjone E , Prydz H
Ref : Biochemical & Biophysical Research Communications , 148 :161 , 1987
Abstract :
PubMedSearch : Rogne_1987_Biochem.Biophys.Res.Commun_148_161
PubMedID: 2823801
Gene_locus related to this paper: human-LCAT