Associated Papers
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
Fibrinogen Saint-Germain II: hypofibrinogenemia due to heterozygous gamma N345S mutation.
de Raucourt E et al.
Thrombosis and Haemostasis, 2005
Congenital hypofibrinogenemia: characterization of two missense mutations affecting fibrinogen assembly and secretion.
Platè M et al.
Blood Cells, Molecules & Diseases, 0
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