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...
Κύριοι συγγραφείς: | Kyriakou, T, Seedorf, U, Goel, A, Hopewell, J, Clarke, R, Watkins, H, Farrall, M |
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Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
Lippincott Williams and Wilkins
2014
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Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
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A common LPA null allele associates with lower lipoprotein(a) levels and coronary artery disease risk.
ανά: Kyriakou, T, κ.ά.
Έκδοση: (2014) -
LPA NULL MUTATION GENOTYPING AND QPCR ANALYSIS REFINE KRINGLE ISOFORM ANALYSIS OF LP(A) LEVELS
ανά: Kyriakou, T, κ.ά.
Έκδοση: (2014) -
Impact of lipoprotein(a) levels and apolipoprotein(a) isoform size on risk of coronary heart disease
ανά: Hopewell, J, κ.ά.
Έκδοση: (2014) -
Impact of lipoprotein(a) levels and apolipoprotein(a) isoform size on risk of coronary heart disease.
ανά: Hopewell, J, κ.ά.
Έκδοση: (2014) -
Association of Apolipoprotein(a) Isoforms With Coronary Heart Disease is Mediated Through Plasma Lipoprotein(a) Levels
ανά: Hopewell, J, κ.ά.
Έκδοση: (2010)