Associated Papers
Clinical and Genetic Characterization of 51 Patients with Congenital Fibrinogen Disorders from China.
Cai Y et al.
Thrombosis and Haemostasis, 2025
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database.
Mohsenian S et al.
Blood Advances, 2024
Congenital fibrinogen disorders: an update.
de Moerloose P et al.
Seminars in Thrombosis and Hemostasis, 2013
The molecular basis of quantitative fibrinogen disorders.
Asselta R et al.
Journal of Thrombosis and Haemostasis : Jth, 2006
Molecular basis of fibrinogen deficiency.
Neerman-Arbez M
Pathophysiology of Haemostasis and Thrombosis, 2006
The molecular mechanisms of congenital hypofibrinogenaemia.
Maghzal GJ et al.
Cellular and Molecular Life Sciences : Cmls, 2004
Autosomal recessive deficiencies of coagulation factors.
Peyvandi F et al.
Reviews in Clinical and Experimental Hematology, 2001
Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes.
Neerman-Arbez M et al.
Human Genetics, 2001
Fibrinogen gene mutations accounting for congenital afibrinogenemia.
Neerman-Arbez M
Annals of the New York Academy of Sciences, 2001
Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia.
Neerman-Arbez M et al.
Blood, 2000
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