QuickView for FGB;jsessionid=825D675C81B4C76125734F0E042C7FB1;jsessionid=E36D1FDB7A0FC6B65A3FB59A834B6652;jsessionid=191ADD0FAF763A2A92899C3E829D0859;jsessionid=D46434F6E84317D5AEAFB0D9E04A412D;jsessionid=1C8F8BDA7818203D3ACAF869FA80506C;jsessionid=1B8EABBF5E06C71C1E42C46024D9FBBB (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=D46434F6E84317D5AEAFB0D9E04A412D;jsessionid=1C8F8BDA7818203D3ACAF869FA80506C;jsessionid=1B8EABBF5E06C71C1E42C46024D9FBBB