Open AccessHereditary thrombophilia by factor V Leiden G1691A (heterozygous) and FII prothrombin G20210A (homozygous) mutations in a patient with ischemic cerebrovascular accident
Author(s) -
Leonardo G. P. Ruiz,
Maria Gabriela Leme de Oliveira,
Adriana L. Z. Ruiz,
Camila S. Daher,
Maurício Lacerda Nogueira
Publication year - 2018
Publication title -
jornal brasileiro de patologia e medicina laboratorial
Language(s) - English
Resource type - Journals
eISSN - 1678-4774
pISSN - 1676-2444
DOI - 10.5935/1676-2444.20180016
Subject(s) - prothrombin g20210a , thrombophilia , medicine , factor v leiden , genetics , factor v , cardiology , gastroenterology , thrombosis , biology , venous thrombosis
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