QuickView for FGG;jsessionid=BF1E356D0D4216E803CBBC7EDD6FC2B5 (gene)

No studies found

1. A case of inherited afibrinogenemia caused by an IVS7-12A>G splice mutation of FGG gene].
2. Fibrinogen Columbus III: A novel c.963del frameshift mutation in the FGG gene resulting in hypofibri…
3. Genetic analysis of two Chinese pedigrees affected with Hereditary hypofibrinemia due to missense va…
4. Molecular characterization of two hypofibrinogenemic patients associated with a novel FGG IVS6+23T>A…
5. Hereditary Hypofibrinogenemia with Hepatic Storage.

There were no clinical trials for FGG;jsessionid=BF1E356D0D4216E803CBBC7EDD6FC2B5