Associated Papers
Clinical phenotype and laboratory characteristics of 93 patients with congenital fibrinogen disorders from unrelated 36 families.
Tian D et al.
Research and Practice in Thrombosis and Haemostasis, 2024
Congenital dysfibrinogenemia misdiagnosed and inappropriately treated as acute fatty liver in pregnancy: A case report and review of literature.
Jia Y et al.
World Journal of Clinical Cases, 2022
Mutations Accounting for Congenital Fibrinogen Disorders: An Update.
Richard M et al.
Seminars in Thrombosis and Hemostasis, 2022
A novel heterozygous mutation (γIIe367Thr) causes congenital dysfibrinogenemia in a Chinese family.
Luo S et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2020
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