Title : Molecular defect in familial lecithin:cholesterol acyltransferase (LCAT) deficiency: a single nucleotide insertion in LCAT gene causes a complete deficient type of the disease - Bujo_1991_Biochem.Biophys.Res.Commun_181_933 |
Author(s) : Bujo H , Kusunoki J , Ogasawara M , Yamamoto T , Ohta Y , Shimada T , Saito Y , Yoshida S |
Ref : Biochemical & Biophysical Research Communications , 181 :933 , 1991 |
Abstract : Bujo_1991_Biochem.Biophys.Res.Commun_181_933 |
ESTHER : Bujo_1991_Biochem.Biophys.Res.Commun_181_933 |
PubMedSearch : Bujo_1991_Biochem.Biophys.Res.Commun_181_933 |
PubMedID: 1662503 |