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Hereditary thrombophilia by factor V Leiden G1691A (heterozygous) and FII prothrombin G20210A (homozygous) mutations in a patient with ischemic cerebrovascular accident by Leonardo G. P. Ruiz, Maria Gabriela L. Oliveira, Adriana L. Z. Ruiz, Camila S. Daher, Mauricio L. Nogueira
Published 2018-04-01
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