Report for Miettinen H

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References (1)

Title : Two different allelic mutations in a Finnish family with lecithin:cholesterol acyltransferase deficiency - Miettinen_1995_Arterioscler.Thromb.Vasc.Biol_15_460
Author(s) : Miettinen H , Gylling H , Ulmanen I , Miettinen TA , Kontula K
Ref : Arterioscler Thromb Vasc Biol , 15 :460 , 1995
Abstract : Miettinen_1995_Arterioscler.Thromb.Vasc.Biol_15_460
ESTHER : Miettinen_1995_Arterioscler.Thromb.Vasc.Biol_15_460
PubMedSearch : Miettinen_1995_Arterioscler.Thromb.Vasc.Biol_15_460
PubMedID: 7749857
Gene_locus related to this paper: human-LCAT