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Owen_1996_Hum.Mutat_8_79

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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

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Citations formats

Owen JS, Wiebusch H, Cullen P, Watts GF, Lima VL, Funke H, Assmann G (1996)
Complete deficiency of plasma lecithin-cholesterol acyltransferase (LCAT) activity due to a novel homozygous mutation (Gly-30-Ser) in the LCAT gene
Hum Mutat 8 :79

Owen JS, Wiebusch H, Cullen P, Watts GF, Lima VL, Funke H, Assmann G (1996)
Hum Mutat 8 :79