A Novel Heterozygous Mutation in FGB (c.1231_1232 del GA) Causing Hypofibrinogenemia With Mild Bleeding in a Large Swiss family

Fuente: Wiley Open Access

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Bibliographic Details
Main Authors:	Sophie Voruz, Jasmine Noetzli, Mathilde Gavillet, Marguerite Neerman‐Arbez, Mattia Rizzi, Lorenzo Alberio, Alessandro Casini
Format:	Artículo Open Access
Published:	Wiley 2025
Subjects:	Haemophilia
Online Access:	Acceder al recurso
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