共 50 条
- [43] Case Report: Novel Mutation of F5 With Maternal Uniparental Disomy Causes Severe Congenital Factor V Deficiency FRONTIERS IN PEDIATRICS, 2022, 10
- [45] Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2008, 93 (10): : 1505 - 1513
- [50] A Novel Botulinum Neurotoxin, Previously Reported as Serotype H, Has a Hybrid-Like Structure With Regions of Similarity to the Structures of Serotypes A and F and Is Neutralized With Serotype A Antitoxin JOURNAL OF INFECTIOUS DISEASES, 2016, 213 (03): : 379 - 385