Factor V gene G1691A mutation, prothrombin gene G20210A mutation, and MTHFR gene C677T mutation are not risk factors for pulmonary thromboembolism in Chinese population-Reference-Cited by-同舟云学术

Factor V gene G1691A mutation, prothrombin gene G20210A mutation, and MTHFR gene C677T mutation are not risk factors for pulmonary thromboembolism in Chinese population

Published:2002-04 Issue:1 Volume:106 Page:7-12
ISSN:0049-3848
Container-title:Thrombosis Research
language:en
Short-container-title:Thrombosis Research

Author:

Lu Yanhui,Zhao Yanfen,Liu Guozhang,Wang Xiaoling,Liu Zhihong,Chen Baiping,Hui Rutai

Publisher

Elsevier BV

Subject

Hematology

Reference23 articles.

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2. Mutation in blood coagulation factor V associated with resistance to activated protein C;Bertina;Nature,1994

3. A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and increase in venous thrombosis;Poort;Blood,1996

4. Prevalence of 20210A allele of the prothrombin gene in venous thromboembolism patients;Leroyer;Thromb Haemostasis,1998

5. The 20210A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis;Hillarp;Thromb Haemostasis,1997

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