The prothrombin G20210A mutation: A new high-prevalence congenital risk factor for thrombosis-Reference-Cited by-同舟云学术

The prothrombin G20210A mutation: A new high-prevalence congenital risk factor for thrombosis

Published:1999-01 Issue:1 Volume:116 Page:213-215
ISSN:0016-5085
Container-title:Gastroenterology
language:en
Short-container-title:Gastroenterology

Author:

Laposata Michael

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference7 articles.

1. Frequent factor II G20210A mutation in idiopathic portal vein thrombosis;Chamouard;Gastroenterology,1999

2. Laboratory evaluation of hypercoagulable states;Van Cott;Hematol Oncol Clin North Am,1998

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

4. The prothrombin gene 3'-untranslated region mutation shows ethnicity-specific variation in allele frequency and is frequently associated with factor V Leiden in thrombophilic patients;Howard;Am J Clin Pathol,1998

5. Geographic distribution of the 20210 G to A prothrombin variant;Rosendaal;Thromb Haemost,1998

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