Associated Papers
Mutations Accounting for Congenital Fibrinogen Disorders: An Update.
Richard M et al.
Seminars in Thrombosis and Hemostasis, 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
Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia.
Casini A et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2017
Select a paper to view details