Associated Papers
Genetic and clinical characterization of congenital fibrinogen disorders in ten Polish patients: identification of three new variants - Fibrinogen Gdańsk II (FGB c.749A>G), Fibrinogen Gdańsk III (FGG c.246dupA) and Fibrinogen Toruń (FGB c.270delT).
Ochotnicka J et al.
Polish Archives of Internal Medicine, 2026
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
Molecular dynamics-based analyses of the structural instability and secondary structure of the fibrinogen gamma chain protein with the D356V mutation.
Ali SK et al.
Journal of Biomolecular Structure & Dynamics, 2017
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