QuickView for FGA;jsessionid=99A47BBCFF75D02249FAB1AEC3EA0BD9;jsessionid=6F10166A557A167E5401F33658D4317C;jsessionid=9A7C804A76833EDCCE3276B2E90AB7E4 (gene)

1. Analysis of an Inherited Dysfibrinogenemia Pedigree Associated with a Heterozygous Mutation in the F…
2. FGA Controls VEGFA Secretion to Promote Angiogenesis by Activating the VEGFR2-FAK Signalling Pathway…
3. A Novel Frameshift Mutation in the FGA Gene (c.196 delT) Leading to Congenital Afibrinogenemia.
4. Afibrinogenemia with two compound heterozygous mutations in FGA gene.
5. Serum Proteomic Analysis Identifies SAA1, FGA, SAP, and CETP as New Biomarkers for Eosinophilic Gran…

There were no clinical trials for FGA;jsessionid=99A47BBCFF75D02249FAB1AEC3EA0BD9;jsessionid=6F10166A557A167E5401F33658D4317C;jsessionid=9A7C804A76833EDCCE3276B2E90AB7E4