Associated Papers
Coexistence of Congenital Dysfibrinogenemia and Antiphospholipid Syndrome in Pregnancy: A Case Report.
Wang Z et al.
International Journal of Women's Health, 2025
Mutations Causing Mild or No Structural Damage in Interfaces of Multimerization of the Fibrinogen γ-Module More Likely Confer Negative Dominant Behaviors.
Bellacchio E
International Journal of Molecular Sciences, 2020
Clinical features and molecular basis of 102 Chinese patients with congenital dysfibrinogenemia.
Zhou J et al.
Blood Cells, Molecules & Diseases, 2015
[Pathogenesis study of inherited dysfibrinogenemia].
Liao Z et al.
Zhonghua Yi Xue Za Zhi, 2014
Fibrinogen Hangzhou: congenital dysfibrinogenemia caused by the novel missense mutation in FGG (γ308Asn→Thr).
Liao Z et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2014
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