A novel mutation in the FGG gene causes hypofibrinogenemia in a Chinese family

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Congenital hypofibrinogenemia with bleeding risk: mutations in the <i>FGA, FGB</i> , and <i>FGG</i> genes2025
2. 2Implications of the c.1201C &gt; G (p.Arg401Gly) mutation in FGG gene on fibrinogen stability and function2025
3. 3Identification of genetic variants in the FGB gene associated with congenital hypofibrinogenemia with divergent clinical phenotype2026
4. 4Hypofibrinogenemia caused by a heterozygous variant in the FGA gene: a case report2026
5. 5Identification and Pathogenicity Analysis of a Novel Fibrinogen Bβ Chain p.Gly293Val Variant Causing Hypofibrinogenemia2026