The significance or nonsignificance of the G to A 20210 prothrombin polymorphism

Clinical and Applied Thrombosis/Hemostasis

Volumn 6, Issue 4, 2000, Pages 239-240

  Girolami, A ^a   Vianello, F ^a  

^a UNIVERSITY OF PADUA MEDICAL SCHOOL   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE; BLOOD CLOTTING FACTOR 5 LEIDEN; GUANINE; PROTHROMBIN;

CLINICAL ARTICLE; DNA POLYMORPHISM; HOMOZYGOSITY; HUMAN; HYPERCOAGULABILITY; IDIOPATHIC DISEASE; IMMUNOASSAY; LETTER; PRIORITY JOURNAL; THROMBOEMBOLISM; VEIN THROMBOSIS;

EID: 0034544620     PISSN: 10760296     EISSN: None     Source Type: Journal    
DOI: 10.1177/107602960000600410     Document Type: Letter

References (16)

1. Review and management of patients with the prothrombin G 20210 A polymorphism
2. Homozygous G20210A prothrombin gene mutation without thromboembolic events: A case report
3. Asymptomatic homozygous nt 20210 G to A prothrombin polymorphism in two blood donors belonging to two different kindreds
4. Two additional homozygous patients for the 20210 prothrombin polymorphism with no venous thrombosis
5. A three generation family presenting five cases of homozygosity for the 20210 G to A prothrombin variant
6. Homozygotes for prothrombin gene 20210 A allele in a thrombophilic family without clinical manifestations of venous thromboembolism
7. Low rate of venous thromboembolism in asymptomatic relatives of probands with Factor V Leiden mutation
8. Associations are not effects
9. G to A 20210 prothrombin polymorphism and venous thrombosis: Simple association or causal relationship?
10. Low incidence of venous thrombosis in homozygous patients with nt 20210 G to A prothrombin polymorphism
11. Clinical and analytical relevance of the combination of prothrombin 201210A/A and factor V Leiden: Results from a large family
12. Papel de los polimorfismos geneticos de los factores de la coagulacion en el sistema hemostatico
13. Prothrombin antigen levels in symptomatic and asymptomatic carriers of the 20210A prothrombin variant
14. Prothrombin and the prothrombin 201210 G to A polymorphism: Their relationship with hypercoagulability and thrombosis
15. It is not sure yet whether the nt 20210 G to A prothrombin polymorphism represents a cause of familial venous thrombophilia
16. 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