Compound heterozygosity for a known (G188E) and novel (W394X) LPL gene mutation causing familial lipoprotein lipase deficiency

G. Crawford, G.F. Wats, K. Robertson, J.R. Burnett, Frank Van Bockxmeer

    Research output: Chapter in Book/Conference paperConference paper

    Original languageEnglish
    Title of host publication74th Congress of the European Atherosclerosis Society
    EditorsE.J. Schaefer
    Place of PublicationIreland
    PublisherElsevier
    PagesNA
    Volume5
    EditionServille, Spain
    ISBN (Print)15675688
    DOIs
    Publication statusPublished - 2004
    EventCompound heterozygosity for a known (G188E) and novel (W394X) LPL gene mutation causing familial lipoprotein lipase deficiency - Serville, Spain
    Duration: 1 Jan 2004 → …

    Conference

    ConferenceCompound heterozygosity for a known (G188E) and novel (W394X) LPL gene mutation causing familial lipoprotein lipase deficiency
    Period1/01/04 → …

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