Molecular characterization of two hypofibrinogenemic patients associated with a novel FGG IVS6+23T>A substitution and a previously reported FGB IVS6-10_16delTTTG deletion
Haemophilia. 2020 Jul;26(4):e194-e197.
doi: 10.1111/hae.13974.
Epub 2020 Mar 23.