GW24-e1722 FOXP3 demethylation as a means of identifying quantitative defects in regulatory T cells in acute coronary syndrome | Heart

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Basic and Translational Medicine

Translational medical research of cardiovascular disease

GW24-e1722 FOXP3 demethylation as a means of identifying quantitative defects in regulatory T cells in acute coronary syndrome

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Cite this article as:: Caixia L, Zhang C

GW24-e1722 FOXP3 demethylation as a means of identifying quantitative defects in regulatory T cells in acute coronary syndrome

Heart 2013;99:A100.