Associated Papers
F9 mutations causing deletions beyond the serine protease domain confer higher risk for inhibitor development in hemophilia B.
Liu G et al.
Blood, 2023
The characteristics and spectrum of F9 mutations in Chinese sporadic haemophilia B pedigrees.
Lu Y et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2019
Molecular characterization of haemophilia B patients in southern Brazil.
Meireles MR et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2017
Select a paper to view details