O K

References (1)

Title : Lecithin:cholesterol acyltransferase deficiency: identification of a causative gene mutation and a co-inherited protein polymorphism - Hill_1993_Biochim.Biophys.Acta_1181_321
Author(s) : Hill JS , O K , Wang X , Pritchard PH
Ref : Biochimica & Biophysica Acta , 1181 :321 , 1993
Abstract : Hill_1993_Biochim.Biophys.Acta_1181_321
ESTHER : Hill_1993_Biochim.Biophys.Acta_1181_321
PubMedSearch : Hill_1993_Biochim.Biophys.Acta_1181_321
PubMedID: 8318557
Gene_locus related to this paper: human-LCAT