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

Voruz, Sophie; Noetzli, Jasmine; Gavillet, Mathilde; Neerman Arbez, Marguerite; Rizzi, Mattia; Alberio, Lorenzo; Casini, Alessandro

doi:10.1111/hae.70185

Scientific article

Letter

English

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

ContributorsVoruz, Sophie; Noetzli, Jasmine; Gavillet, Mathilde; Neerman Arbez, Marguerite

; Rizzi, Mattia; Alberio, Lorenzo; Casini, Alessandro

Published inHaemophilia, vol. 32, no. 1, p. 344-347

Publication date2026

First online date2025-12-17

Affiliation entities

Faculté de médecine / Section de médecine clinique / Département de médecine
Faculté de médecine / Section de médecine fondamentale / Département de médecine génétique et développement

Research groups

Citation (ISO format)

VORUZ, Sophie et al. A Novel Heterozygous Mutation in FGB (c.1231_1232 del GA) Causing Hypofibrinogenemia With Mild Bleeding in a Large Swiss family. In: Haemophilia, 2026, vol. 32, n° 1, p. 344–347. doi: 10.1111/hae.70185

Article (Published version)

Identifiers

PID : unige:195168
DOI : 10.1111/hae.70185
PMID : 41403363

Journal ISSN1351-8216

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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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