Coagulation Factor IX Propeptide Mutations Causing Coumarin Hypersensitivity: Identification of Female Alanine-10 Valine Heterozygotes
Author:
Publisher
Georg Thieme Verlag KG
Subject
Hematology
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0037-1615629.pdf
Cited by 23 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. 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;Thrombosis Research;2019-02
2. Variants in FIX propeptide associated with vitamin K antagonist hypersensitivity: functional analysis and additional data confirming the common founder mutations;Annals of Hematology;2018-02-15
3. The importance of genetic factors for the development of arthropathy: a longitudinal study of children and adolescents with haemophilia A;Thrombosis and Haemostasis;2017
4. Factor IX propeptide mutation and life threatening bleeding;Thrombosis Research;2011-11
5. Life-threatening bleeding under vitamin K antagonists in spite of an INR in the therapeutic range;Journal of Thrombosis and Thrombolysis;2011-03-18
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