Increased prevalence of the G20210A prothrombin gene variant in acute coronary syndromes without metabolic or acquired risk factors or with limited extent of disease | Zendy

Francesco Burzotta | Zendy

Open Access

Increased prevalence of the G20210A prothrombin gene variant in acute coronary syndromes without metabolic or acquired risk factors or with limited extent of disease

Author(s) -

Francesco Burzotta

Publication year - 2002

Publication title -

european heart journal

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 4.336

H-Index - 293

eISSN - 1522-9645

pISSN - 0195-668X

DOI - 10.1053/euhj.2001.2685

Subject(s) - medicine , risk factor , prothrombin g20210a , factor v leiden , disease , cardiology , acute coronary syndrome , coronary artery disease , gene , thrombosis , genetics , myocardial infarction , venous thrombosis , biology

To investigate the prevalence of the G20210A prothrombin and G1691A factor V gene variants in patients with acute coronary syndrome stratified according to risk factor profile and to extent of coronary disease, in comparison with matched healthy controls.

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