CONGENITAL OCCIPITAL MENINGOENCEPHALOCELE AND MTHFR - C677T MUTATION IN HETEROZIGOSIS - CASE REPORT
نویسندگان
چکیده
منابع مشابه
Factor V Leiden, MTHFR C677T and Prothrombin Gene Mutation G20210A in Iranian Patients with Venous Thrombosis
Background: Factor V Leiden, Prothrombin gene (G20210A) and MTHFR (C677T) polymorphism are the main biomarkers for evaluation of tendency for venous thromboembolism. We aimed to investigate the frequency of mutations in factor V Leiden, Prothrombin G20210A and MTHFR C677T and identify the genetic status for these mutations in patients with venous thrombosis. Methods: This study was carried out...
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ژورنال
عنوان ژورنال: Revista Brasileira de Ultrassonografia
سال: 2020
ISSN: 2675-4800
DOI: 10.17648/rbus-v28n29-7