Bujo_1991_Biochem.Biophys.Res.Commun_181_933

Reference

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

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Citations formats

Bujo H, Kusunoki J, Ogasawara M, Yamamoto T, Ohta Y, Shimada T, Saito Y, Yoshida S (1991)
Molecular defect in familial lecithin:cholesterol acyltransferase (LCAT) deficiency: a single nucleotide insertion in LCAT gene causes a complete deficient type of the disease
Biochemical & Biophysical Research Communications 181 :933

Bujo H, Kusunoki J, Ogasawara M, Yamamoto T, Ohta Y, Shimada T, Saito Y, Yoshida S (1991)
Biochemical & Biophysical Research Communications 181 :933