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Funding This paper was supported by San Matteo Hospital Foundation, Internal Medicine research fundings, PRIN2017. Publishers note All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers
Hotez PJ, Molyneux DH, Fenwick A, Ottesen E, Ehrlich Sachs S, et al
However, variant allele 198L of the GPX1 gene tended to be associated with an increased risk of CS in hypertensive patients (OR=1.26, 95%CI 0.991.60, P =0.06, P adj =0.18)
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