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Familial Dysfibrinogenemia Due to FGG Mutation with Variable Bleeding PhenotypeDOI 10.1007/s12288-026-02537-x
Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management.Semantic proximity
[FGA gene variation causing congenital dysfibrinogenemia with recurrent arteriovenous thrombosis].Semantic proximity
Congenital dysfibrinogenemia Aα Gly13Glu associated with bleeding during pregnancy.Semantic proximity
Analysis of an Inherited Dysfibrinogenemia Pedigree Associated with a Heterozygous Mutation in the FGA Gene.Semantic proximity
Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia.Semantic proximity
Congenital dysfibrinogenemia caused by a heterozygous mutation in the FGA gene: A case report and review of literatureSemantic proximity
Heterogeneity of Genotype–Phenotype in Congenital Hypofibrinogenemia—A Review of Case Reports Associated with Bleeding and ThrombosisSemantic proximity
A novel mutation in the FGG gene causes hypofibrinogenemia in a Chinese family.Semantic proximity
[A Family with Congenital Dysfibrinogenemia and Blood Transfusion].Semantic proximity
Genetic mutations associated with congenital fibrinogen disorders: global distribution and clinical outcomes.Semantic proximity
Fibrinogen Columbus III: A novel c.963del frameshift mutation in the FGG gene resulting in hypofibrinogenemia with a bleeding phenotype.Semantic proximity
Risk of bleeding and thrombosis in inherited qualitative fibrinogen disordersSemantic proximity
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