QuickView for FGB;jsessionid=825D675C81B4C76125734F0E042C7FB1;jsessionid=E36D1FDB7A0FC6B65A3FB59A834B6652;jsessionid=191ADD0FAF763A2A92899C3E829D0859;jsessionid=C4B881AE516BE81CD447A80B6A9EC021;jsessionid=D7777B0D1142CE963EDE794006E790E2 (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. Congenital fibrinogen disorder with a compound heterozygote possessing two novel FGB mutations, one …
4. Genetic Analysis of Afibrinogenemia and Hypofibrinogenemia: Novel Mutations in the FGB Gene in the T…
5. A novel deletion in the fibrinogen beta chain (FGB) gene causing hypofibrinogenemia.

There were no clinical trials for FGB;jsessionid=825D675C81B4C76125734F0E042C7FB1;jsessionid=E36D1FDB7A0FC6B65A3FB59A834B6652;jsessionid=191ADD0FAF763A2A92899C3E829D0859;jsessionid=C4B881AE516BE81CD447A80B6A9EC021;jsessionid=D7777B0D1142CE963EDE794006E790E2