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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 HE, Gylling H, Tenhunen J, Virtamo J, Jauhiainen M, Huttunen JK, Kantola I, Miettinen TA, Kontula K. Miettinen HE, et al. Among authors: tenhunen j. Arterioscler Thromb Vasc Biol. 1998 Apr;18(4):591-8. doi: 10.1161/01.atv.18.4.591. Arterioscler Thromb Vasc Biol. 1998. PMID: 9555865
233 results