Associated Papers
Three new variants of the fibrinogen-related domain of the fibrinogen Bβ chain.
Kotlín R et al.
Thrombosis Research, 2025
A heterozygous nonsense mutation in the FGB gene (c.1299G > A) causes congenital fibrinogen disorder across four consecutive generations.
Chen W et al.
Thrombosis Journal, 2025
Structural and Functional Characterization of Four Novel Fibrinogen Mutations in FGB Causing Congenital Fibrinogen Disorder.
Ceznerová E et al.
International Journal of Molecular Sciences, 2022
The β-chain mutation p.Trp433Stop impairs fibrinogen secretion: A novel nonsense mutation associated with hypofibrinogenemia.
Yan J et al.
International Journal of Laboratory Hematology, 2021
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