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Author Report for: Kontula K

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    Title: Association of lipoprotein lipase Ser447Ter polymorphism with brain infarction: a population-based neuropathological study
    Myllykangas L, Polvikoski T, Sulkava R, Notkola IL, Rastas S, Verkkoniemi A, Tienari PJ, Niinisto L, Hardy J and Haltia M <2 more author(s)>
    Ref: Ann Med, 33:486, 2001 : PubMed

            

    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 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 : PubMed

            

    Title: Two different allelic mutations in a Finnish family with lecithin:cholesterol acyltransferase deficiency
    Miettinen H, Gylling H, Ulmanen I, Miettinen TA, Kontula K
    Ref: Arterioscler Thromb Vasc Biol, 15:460, 1995 : PubMed

            

    Title: A novel amino acid substitution (His183-->Gln) in exon 5 of the lipoprotein lipase gene results in loss of catalytic activity: phenotypic expression of the mutant gene in a heterozygous state
    Tenkanen H, Taskinen MR, Antikainen M, Ulmanen I, Kontula K, Ehnholm C
    Ref: J Lipid Res, 35:220, 1994 : PubMed

            


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