Associated Papers
Translational readthrough at F8 nonsense variants in the factor VIII B domain contributes to residual expression and lowers inhibitor association.
Testa MF et al.
Haematologica, 2023
35924581 (PubMed )
Supplement: 2022_281279_TESTA_SUPPL.pdf
Identification of novel mutations in exon 14 of the f8 gene in malaysian patients with severe hemophilia a.
Moses EJ et al.
Indian Journal of Clinical Biochemistry : Ijcb, 2012
Spectrum of mutations in Albanian patients with haemophilia A: identification of ten novel mutations in the factor VIII gene.
Castaman G et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2007
Select a paper to view details