Associated Papers
Congenital hypofibrinogenemia with bleeding risk: mutations in the FGA, FGB, and FGG genes.
Wu Y et al.
Laboratory Medicine, 2026
Molecular characterization of two hypofibrinogenemic patients associated with a novel FGG IVS6+23T>A substitution and a previously reported FGB IVS6-10_16delTTTG deletion.
Amri Y et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2020
In vitro transcription of compound heterozygous hypofibrinogenemia Matsumoto IX; first identification of FGB IVS6 deletion of 4 nucleotides and FGG IVS3-2A>G causing abnormal RNA splicing.
Terasawa F et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2010
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