Associated Papers
Fibrinogen Mahdia: A congenitally abnormal fibrinogen characterized by defective fibrin polymerization.
Amri Y et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2017
The molecular basis of quantitative fibrinogen disorders.
Asselta R et al.
Journal of Thrombosis and Haemostasis : Jth, 2006
Fibrinogen Seoul (FGG Ala341Asp): a novel mutation associated with hypodysfibrinogenemia.
Song KS et al.
Clinical and Applied Thrombosis/hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/hemostasis, 2006
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
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