Severe bleeding due to hypersensitivity to vitamin K antagonist caused by the c.109G>A (p.Ala37Thr) mutation in the F9 gene in a patient with mechanical heart valve prosthesis-Reference-Cited by-同舟云学术

Severe bleeding due to hypersensitivity to vitamin K antagonist caused by the c.109G>A (p.Ala37Thr) mutation in the F9 gene in a patient with mechanical heart valve prosthesis

Published:2019-02 Issue: Volume:174 Page:59-61
ISSN:0049-3848
Container-title:Thrombosis Research
language:en
Short-container-title:Thrombosis Research

Author:

Odnoczko Edyta^ORCID,Falkowska Joanna,Baran Beata,Buczma Anna,Stefanska-Windyga Ewa,Windyga Jerzy

Funder

Institute of Hematology and Transfusion Medicine, Warsaw, Poland

Publisher

Elsevier BV

Subject

Hematology

Reference14 articles.

1. Missense mutations at ALA-10 in the factor IX propeptide: an insignificant variant in normal life but a decisive cause of bleeding during oral anticoagulant therapy;Oldenburg;Br. J. Haematol.,1997

2. A mutation in the propeptide of factor IX leads to warfarin sensitivity by a novel mechanism;Chu;J. Clin. Invest.,1996

3. Genetic predisposition to bleeding during oral anticoagulant therapy: evidence for common founder mutations (FIXVal-10 and FIXThr-10) and an independent CpG hotspot mutation (FIXThr-10);Oldenburg;Thromb. Haemost.,2001

4. Congenital hypersensitivity to vitamin K antagonists due to FIX propeptide mutation at locus-10: a (not so) rare cause of bleeding under oral anticoagulant therapy in Switzerland;Ulrich;Swiss Med. Wkly.,2008

5. Coagulation factor IX propeptide mutations causing coumarin hypersensitivity: identification of female alanine-10 valine heterozygotes;Bestmann;Thromb. Haemost.,2001

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