QuickView for FGB;jsessionid=825D675C81B4C76125734F0E042C7FB1;jsessionid=E36D1FDB7A0FC6B65A3FB59A834B6652 (gene)

1. Analysis of two pedigrees affected with inherited dysfibrinogenemia due to a novel c.1115 T>A varian…
2. miR-139-5p Suppresses Proliferation and Angiogenesis of Intracranial Aneurysm via FGB.
3. Circ_16601 facilitates Hippo pathway signaling via the miR-5580-5p/FGB axis to promote my-CAF recrui…
4. Congenital fibrinogen disorder with a compound heterozygote possessing two novel FGB mutations, one …
5. Genetic Analysis of Afibrinogenemia and Hypofibrinogenemia: Novel Mutations in the FGB Gene in the T…

There were no clinical trials for FGB;jsessionid=825D675C81B4C76125734F0E042C7FB1;jsessionid=E36D1FDB7A0FC6B65A3FB59A834B6652