Articles with "rs28362680" as a keyword



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Missense Variant rs28362680 in BTNL2 Reduces Risk of Coronary Heart Disease

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Published in 2022 at "Pharmacogenomics and Personalized Medicine"

DOI: 10.2147/pgpm.s353085

Abstract: Background The pathological basis of coronary heart disease (CHD) is atherosclerosis. BTNL2 can inhibit the activation of T cells. We aimed to explore the association between BTNL2 genetic variants and CHD risk in the southern… read more here.

Keywords: rs28362680; missense; chd risk; analysis ... See more keywords