Associated Papers
Clinical, biological, and genetic features in an afibrinogenemia patient series in Algeria.
Hadjali-Saichi S et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2022
Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype.
Simurda T et al.
International Journal of Molecular Sciences, 2020
FGB mutations leading to congenital quantitative fibrinogen deficiencies: an update and report of four novel mutations.
Casini A et al.
Thrombosis Research, 2014
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