Barely Significant
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Acute Myocardial Infarction in Patients with Hereditary Thrombophilia-A Focus on Factor V Leiden and Prothrombin G20210A.

Life (Basel) · 2023 · PMC10300874 · PMID 37374153

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highly significantno p-value reported
They provided the first clear indication of the existence of a moderate and highly significant increase in per-allele relative risk for MI in FV Leiden and/or prothrombin G20210A carriers.

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