The A20210 allele of the prothrombin gene is frequently associated with the factor V Arg 506 to Gln mutation but not with protein S deficiency in thrombophilic families

被引：51

作者：

Zöller, B

Svensson, PJ

Dahlbäck, B

Hillarp, A

机构：

[1] Univ Lund Hosp, Dept Internal Med, S-22185 Lund, Sweden

[2] Univ Lund Hosp, Dept Coagulat Disorders, Malmo, Sweden

[3] Univ Lund Hosp, Dept Clin Chem, Malmo, Sweden

来源：

BLOOD | 1998年 / 91卷 / 06期

关键词：

D O I：

10.1182/blood.V91.6.2210

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：2210 / 2211

页数：2

共 9 条

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[2] Risk of venous thromboembolism associated with a G to A transition at position 20210 in the 3'-untranslated region of the prothrombin gene [J].

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[3] The venous thrombosis risk factor 20210 A allele of the prothrombin gene is not a major risk factor for arterial thrombotic disease [J].

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[5]

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[6]

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[8] EVALUATION OF THE RELATIONSHIP BETWEEN PROTEIN-S AND C4B-BINDING PROTEIN ISOFORMS IN HEREDITARY PROTEIN-S DEFICIENCY DEMONSTRATING TYPE-I AND TYPE-III DEFICIENCIES TO BE PHENOTYPIC VARIANTS OF THE SAME GENETIC-DISEASE [J].

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[9] IDENTIFICATION OF THE SAME FACTOR-V GENE MUTATION IN 47 OUT OF 50 THROMBOSIS-PRONE FAMILIES WITH INHERITED RESISTANCE TO ACTIVATED PROTEIN-C [J].

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