Search Results - "Faegeman, O."

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  1. 1
    Binding defective low density lipoprotein identified in subjects with specific polymorphisms of the apolipoprotein B gene

    Binding defective low density lipoprotein identified in subjects with specific polymorphisms of the apolipoprotein B gene by Heath, F., Hansen, P.S., Gerdes, L.U., Jensen, T.G., Jensen, L.G., Jensen, H.K., Gregersen, N., Kølvraa, S., Bolund, L., Faegeman, O.

    Published in Atherosclerosis (01-06-1995)
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  2. 2
    The Trp23-stop and Trp66-Gly mutations in the LDL receptor gene : common causes of familial hypercholesterolemia in Denmark

    The Trp23-stop and Trp66-Gly mutations in the LDL receptor gene : common causes of familial hypercholesterolemia in Denmark by JENSEN, H. K, JENSEN, L. G, HANSEN, P. S, FAEGEMAN, O, GREGERSEN, N

    Published in Atherosclerosis (01-02-1996)
    “…Mutations in the gene for the low density lipoprotein (LDL) receptor cause the autosomal dominant disease familial hypercholesterolemia (FH), the prevalence of…”
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