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...
Main Authors: | Kyriakou, T, Seedorf, U, Goel, A, Hopewell, J, Clarke, R, Watkins, H, Farrall, M |
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פורמט: | Journal article |
שפה: | English |
יצא לאור: |
Lippincott Williams and Wilkins
2014
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פריטים דומים
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A common LPA null allele associates with lower lipoprotein(a) levels and coronary artery disease risk.
מאת: Kyriakou, T, et al.
יצא לאור: (2014) -
LPA NULL MUTATION GENOTYPING AND QPCR ANALYSIS REFINE KRINGLE ISOFORM ANALYSIS OF LP(A) LEVELS
מאת: Kyriakou, T, et al.
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Impact of lipoprotein(a) levels and apolipoprotein(a) isoform size on risk of coronary heart disease
מאת: Hopewell, J, et al.
יצא לאור: (2014) -
Impact of lipoprotein(a) levels and apolipoprotein(a) isoform size on risk of coronary heart disease.
מאת: Hopewell, J, et al.
יצא לאור: (2014) -
Association of Apolipoprotein(a) Isoforms With Coronary Heart Disease is Mediated Through Plasma Lipoprotein(a) Levels
מאת: Hopewell, J, et al.
יצא לאור: (2010)