Title : Molecular genetic study of Finns with hypoalphalipoproteinemia and hyperalphalipoproteinemia: a novel Gly230 Arg mutation (LCAT[Fin]) of lecithin:cholesterol acyltransferase (LCAT) accounts for 5\% of cases with very low serum HDL cholesterol levels - Miettinen_1998_Arterioscler.Thromb.Vasc.Biol_18_591 |
Author(s) : Miettinen HE , Gylling H , Tenhunen J , Virtamo J , Jauhiainen M , Huttunen JK , Kantola I , Miettinen TA , Kontula K |
Ref : Arterioscler Thromb Vasc Biol , 18 :591 , 1998 |
Abstract : Miettinen_1998_Arterioscler.Thromb.Vasc.Biol_18_591 |
ESTHER : Miettinen_1998_Arterioscler.Thromb.Vasc.Biol_18_591 |
PubMedSearch : Miettinen_1998_Arterioscler.Thromb.Vasc.Biol_18_591 |
PubMedID: 9555865 |
Miettinen HE, Gylling H, Tenhunen J, Virtamo J, Jauhiainen M, Huttunen JK, Kantola I, Miettinen TA, Kontula K (1998)
Molecular genetic study of Finns with hypoalphalipoproteinemia and hyperalphalipoproteinemia: a novel Gly230 Arg mutation (LCAT[Fin]) of lecithin:cholesterol acyltransferase (LCAT) accounts for 5\% of cases with very low serum HDL cholesterol levels
Arterioscler Thromb Vasc Biol
18 :591
Miettinen HE, Gylling H, Tenhunen J, Virtamo J, Jauhiainen M, Huttunen JK, Kantola I, Miettinen TA, Kontula K (1998)
Arterioscler Thromb Vasc Biol
18 :591