Associated Papers
Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation.
Casini A et al.
Journal of Thrombosis and Haemostasis : Jth, 2017
Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutations.
Castaman G et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2008
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