Associated Papers
Mutations Accounting for Congenital Fibrinogen Disorders: An Update.
Richard M et al.
Seminars in Thrombosis and Hemostasis, 2022
A Novel Amino Acid Substitution, Fibrinogen Bβp.Pro234Leu, Associated with Hypofibrinogenemia Causing Impairment of Fibrinogen Assembly and Secretion.
Kaido T et al.
International Journal of Molecular Sciences, 2020
The fibrinogen FGG p.Gly242Glu: a rare mutation associated with hypofibrinogenemia.
Bauduer F et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2018
A novel mutation in the fibrinogen γ-chain 216 Gly>Glu causes hypofibrinogenemia.
Marchi R et al.
Thrombosis Research, 2016
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