Associated Papers
Mutations Accounting for Congenital Fibrinogen Disorders: An Update.
Richard M et al.
Seminars in Thrombosis and Hemostasis, 2022
Mutational Epidemiology of Congenital Fibrinogen Disorders.
Casini A et al.
Thrombosis and Haemostasis, 2018
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
Succession of splicing regulatory elements determines cryptic 5΄ss functionality.
Brillen AL et al.
Nucleic Acids Research, 2017
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