Hereditary thrombophilia by factor V Leiden G1691A (heterozygous) and FII prothrombin G20210A (homozygous) mutations in a patient with ischemic cerebrovascular accident

• 主要な著者: Leonardo G. P. Ruiz (著者), Maria Gabriela L. Oliveira (著者), Adriana L. Z. Ruiz (著者), Camila S. Daher (著者), Mauricio L. Nogueira (著者)
• フォーマット: 図書
• 出版事項: Sociedade Brasileira de Patologia Clínica, 2018-04-01T00:00:00Z.
• 主題: article
• オンライン･アクセス: Connect to this object online.

ABSTRACT Mutations related to Factor V Leiden (G1691A) and prothrombin (G20210A) are associated with a significantly increased risk of venous thromboembolism. The identification of a patient affected by episodes of venous thromboembolism and carrier of G1691A (heterozygous) and G20210A (homozygous)...