Haemophilia : the official journal of the World Federation of Hemophilia
A Novel Heterozygous Mutation in FGB (c.1231_1232 del GA) Causing Hypofibrinogenemia With Mild Bleeding in a Large Swiss family.
Sophie Voruz, Jasmine Noetzli, Mathilde Gavillet, Marguerite Neerman-Arbez, Mattia Rizzi, Lorenzo Alberio, Alessandro Casini
Published: 202510.1111/hae.70185
No abstract available for this study.