A Novel Heterozygous Mutation in FGB (c.1231_1232 del GA) Causing Hypofibrinogenemia With Mild Bleeding in a Large Swiss family.
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| Title: | A Novel Heterozygous Mutation in FGB (c.1231_1232 del GA) Causing Hypofibrinogenemia With Mild Bleeding in a Large Swiss family. |
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| Authors: | Voruz, Sophie1 (AUTHOR), Noetzli, Jasmine1 (AUTHOR), Gavillet, Mathilde1 (AUTHOR), Neerman‐Arbez, Marguerite2 (AUTHOR), Rizzi, Mattia3 (AUTHOR), Alberio, Lorenzo1 (AUTHOR) Lorenzo.Alberio@chuv.ch, Casini, Alessandro4 (AUTHOR) |
| Source: | Haemophilia. Jan/Feb2026, Vol. 32 Issue 1, p344-347. 4p. |
| Database: | Academic Search Ultimate |
| ISSN: | 13518216 |
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| DOI: | 10.1111/hae.70185 |
