Molecular characterization of two hypofibrinogenemic patients associated with a novel FGG IVS6+23T>A substitution and a previously reported FGB IVS6-10_16delTTTG deletion.
Yessine AmriRym DabboubiFathia MghaiethMohamed ZiliTaieb MessaoudAlessandro CasiniPhilippe De MoerlooseNour El Houda ToumiPublished in: Haemophilia : the official journal of the World Federation of Hemophilia (2020)