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Volumn 44, Issue 1, 1999, Pages 13-18

20210 A mutation of the prothrombin and venous thromboembolism gene;Mutacion 20210A del gen de la protrombina y tromboembolismo venoso

Author keywords

[No Author keywords available]

Indexed keywords

PROTHROMBIN;

EID: 0033070536     PISSN: 00364355     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)

References (16)
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  • 2
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  • 3
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  • 4
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    • The 20210 A allele of the prothrombin gene is a common risk factor among swedish outpatients with verified deep venous thrombosis
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  • 5
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    • The venous thrombosis risk factor 20210 A allele of the prothrombin gene is not a major risk factor for arterial thrombotic disease
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  • 6
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  • 7
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  • 8
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    • Martinelli I, Franchi F, Akwan S, Bettini P, Merati G, Mannucci PM. The transition G to A at position 20210 in the 3′-Untranslated region of the prothrombin gene is not associated with cerebral ischaemia. Blood 1997; 90: 3806.
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  • 9
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    • Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients
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  • 10
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  • 12
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  • 14
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    • The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease
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    • Frequencies of prothrombin 20120 G-A mutation may be different among races-studies on Japanese populations with various forms of thrombotic disorders and healthy subjects
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.