Associated Papers
Mutations Accounting for Congenital Fibrinogen Disorders: An Update.
Richard M et al.
Seminars in Thrombosis and Hemostasis, 2022
Whole Blood Thromboelastometry by ROTEM and Thrombin Generation by Genesia According to the Genotype and Clinical Phenotype in Congenital Fibrinogen Disorders.
Szanto T et al.
International Journal of Molecular Sciences, 2021
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
Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation.
Casini A et al.
Journal of Thrombosis and Haemostasis : Jth, 2017
Clinical features and molecular basis of 102 Chinese patients with congenital dysfibrinogenemia.
Zhou J et al.
Blood Cells, Molecules & Diseases, 2015
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