Search Results - "Wright, WT"

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  1. 1

    SNPs at the APOA5 gene account for the strong association with hypertriglyceridaemia at the APOA5/ A4/ C3/ A1 locus on chromosome 11q23 in the Northern Irish population by Wright, William T., Young, Ian S., Nicholls, D. Paul, Patterson, Chris, Lyttle, Kelly, Graham, Colin A.

    Published in Atherosclerosis (01-04-2006)
    “…Serum triglyceride levels (TG) are important independent risk factors for coronary heart disease. The apolipoproteins C-III (apoCIII) and A-V (apoAV) are…”
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    Journal Article
  2. 2

    Multiplex MassARRAY spectrometry (iPLEX) produces a fast and economical test for 56 familial hypercholesterolaemia-causing mutations by Wright, WT, Heggarty, SV, Young, IS, Nicholls, DP, Whittall, R, Humphries, SE, Graham, CA

    Published in Clinical genetics (01-11-2008)
    “…Familial hypercholesterolaemia (FH) is a common single gene disorder, pre‐disposing to cardiovascular disease, which is most commonly caused by mutations in…”
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    Journal Article
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