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...
| Päätekijät: | , , , , , , |
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| Aineistotyyppi: | Journal article |
| Kieli: | English |
| Julkaistu: |
Lippincott Williams and Wilkins
2014
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A common LPA null allele associates with lower lipoprotein(a) levels and coronary artery disease risk.
Julkaistu 2014
Journal article