Association of genetic variants in the HDL receptor, SR-B1, with abnormal lipids in women with coronary artery disease.

Autor: McCarthy, J.J., Lehner, T., Reeves, C., Moliterno, D.J., Newby, L.K., Rogers, W.J., Topol, E.J.
Předmět:
Zdroj: Journal of Medical Genetics; Jun2003, Vol. 40 Issue 6, p453-458, 6p, 2 Charts, 2 Graphs
Abstrakt: Examines polymorphisms in the gene for the high density lipoprotein (HDL) receptor, SR-B1 (SCARB 1), to determine their association with plasma lipids. Evaluation in 371 white coronary artery disease women patients of the association of the four most common polymorphisms in SCARB1 with HDL cholesterol, triglyceride levels and their ratio.
Databáze: Complementary Index