The Prothrombin 20210 A Allele Is Frequently Coinherited in Young Carriers of the Factor V Arg 506 to Gln Mutation With Venous Thrombophilia
Author:
Affiliation:
1. Department of Internal Medicine University Hospital Frankfurt, Germany
2. Department of Pediatrics University Hospital Münster, Germany
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/91/6/2209/1421295/2209.pdf
Reference20 articles.
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2. Mutation in blood coagulation factor V associated with resistance to activated protein C.;Bertina;Nature,1994
3. Activated protein C resistance caused by Arg506Gln mutation in factor Va.;Greengard;Lancet,1994
4. Inherited thrombophilia: Part 1.;Lane;Thromb Haemost,1996
5. Inherited predisposition to thrombosis.;Miletich;Cell,1993
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