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| 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 |