Report for Lima VL

General

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References (2)

Title : Complete deficiency of plasma lecithin-cholesterol acyltransferase (LCAT) activity due to a novel homozygous mutation (Gly-30-Ser) in the LCAT gene -

Author(s) : Owen JS , Wiebusch H , Cullen P , Watts GF , Lima VL , Funke H , Assmann G

Ref : Hum Mutat , 8 :79 , 1996

PubMedID: 8807342

Title : A study of the structure of the gene for lecithin: cholesterol acyltransferase in four unrelated individuals with familial lecithin: cholesterol acyltransferase deficiency - Humphries_1988_Clin.Sci.(Lond)_74_91

Author(s) : Humphries SE , Chaves ME , Tata F , Lima VL , Owen JS , Borysiewicz LK , Catapano A , Vergani C , Gjone E , Clemens MR , et al.

Ref : Clinical Science (Lond) , 74 :91 , 1988

Abstract : Humphries_1988_Clin.Sci.(Lond)_74_91

ESTHER : Humphries_1988_Clin.Sci.(Lond)_74_91

PubMedSearch : Humphries_1988_Clin.Sci.(Lond)_74_91

PubMedID: 3338256

Report for Lima VL

General

References (2)

1. Complete deficiency of plasma lecithin-cholesterol acyltransferase (LCAT) activity due to a novel homozygous mutation (Gly-30-Ser) in the LCAT gene

2. A study of the structure of the gene for lecithin: cholesterol acyltransferase in four unrelated individuals with familial lecithin: cholesterol acyltransferase deficiency