Fibrinogen BOE II: Intracerebral hemorrhage associated with a novel compound mutation in a Chinese family with dysfibrinogenemia
Author:
Publisher
Elsevier BV
Subject
Hematology
Reference11 articles.
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2. Identification of two novel fibrinogen Bβ chain mutations in two Slovak families with quantitative fibrinogen disorders;Simurda;Int. J. Mol. Sci.,2017
3. Laboratory and genetic investigation of mutations accounting for congenital fibrinogen disorders;Neerman-Arbez;Semin. Thromb. Hemost.,2016
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Cited by 3 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. Fibrinogen BOE II: dysfibrinogenemia with bleeding and defective thrombin binding;Research and Practice in Thrombosis and Haemostasis;2023-07
2. Congenital Fibrinogen Disorders, Diagnosis, and Management;Congenital Bleeding Disorders;2023
3. Mutations Accounting for Congenital Fibrinogen Disorders: An Update;Seminars in Thrombosis and Hemostasis;2022-01-24
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