Associated Papers
Clinical features and genetic defect in six index patients with congenital fibrinogen disorders: Three novel mutations with one common mutation in Taiwan's population.
Shen MC et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2021
Combined congenital dysfibrinogenemia and factor VII deficiency from mutations in the FGB and F7 genes.
Woo HI et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2012
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