A common LPA null allele associates with lower lipoprotein(a) levels and coronary artery disease risk
OBJECTIVE - Increased levels of lipoprotein(a) are a highly heritable risk factor for coronary artery disease (CAD). The genetic determinants of lipoprotein(a) levels are mainly because of genetic variation in the apolipoprotein(a) gene (LPA). We have tested the association of a relatively common nu...
المؤلفون الرئيسيون: | Kyriakou, T, Seedorf, U, Goel, A, Hopewell, J, Clarke, R, Watkins, H, Farrall, M |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
Lippincott Williams and Wilkins
2014
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مواد مشابهة
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A common LPA null allele associates with lower lipoprotein(a) levels and coronary artery disease risk.
حسب: Kyriakou, T, وآخرون
منشور في: (2014) -
LPA NULL MUTATION GENOTYPING AND QPCR ANALYSIS REFINE KRINGLE ISOFORM ANALYSIS OF LP(A) LEVELS
حسب: Kyriakou, T, وآخرون
منشور في: (2014) -
Impact of lipoprotein(a) levels and apolipoprotein(a) isoform size on risk of coronary heart disease
حسب: Hopewell, J, وآخرون
منشور في: (2014) -
Impact of lipoprotein(a) levels and apolipoprotein(a) isoform size on risk of coronary heart disease.
حسب: Hopewell, J, وآخرون
منشور في: (2014) -
Association of Apolipoprotein(a) Isoforms With Coronary Heart Disease is Mediated Through Plasma Lipoprotein(a) Levels
حسب: Hopewell, J, وآخرون
منشور في: (2010)