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Lima VL

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 :
PubMedSearch : Humphries_1988_Clin.Sci.(Lond)_74_91
PubMedID: 3338256