Characterisation of a novel thrombomodulin c.1487delC,p.(Pro496Argfs*10) variant and evaluation of therapeutic strategies to manage the rare bleeding phenotype
Author:
Funder
National Institute for Health Research
Publisher
Elsevier BV
Subject
Hematology
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4. Identification of an endothelial cell cofactor for thrombin-catalyzed activation of protein C;Esmon;Proc. Natl. Acad. Sci. U. S. A.,1981
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Cited by 2 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. Management of rare inherited bleeding disorders: Proposals of the French Reference Centre on Haemophilia and Rare Coagulation Disorders;European Journal of Haematology;2023-02-20
2. A novel homozygous variant of the thrombomodulin gene causes a hereditary bleeding disorder;Blood Advances;2021-09-02
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