Associated Papers
Anti-FVIII antibodies in Black and White hemophilia A subjects: do F8 haplotypes play a role?
Pratt KP et al.
Blood Advances, 2023
36459498 (PubMed )
Supplement: BLOODA_ADV-2021-004909-mmc2.xlsx › SHA_BLACK_H1H2_NOINHHIS
Prediction of hemophilia A severity using a small-input machine-learning framework.
Lopes TJS et al.
Npj Systems Biology and Applications, 2021
34035274 (PubMed )
Supplement: 41540_2021_183_MOESM3_ESM.xlsx › Predictions___Clinical_reports
Compensated pathogenic variants in coagulation factors VIII and IX present complex mapping between molecular impact and hemophilia severity.
Marín Ò et al.
Scientific Reports, 2019
31267011 (PubMed )
Supplement: 41598_2019_45916_MOESM2_ESM.xlsx › Variants_used
Usefulness of an in vitro cellular expression model for haemophilia A carrier diagnosis: illustration with five novel mutations in the F8 gene in women with isolated factor VIII:C deficiency.
Roualdes O et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2015
Detection of 95 novel mutations in coagulation factor VIII gene F8 responsible for hemophilia A: results from a single institution.
Guillet B et al.
Human Mutation, 2006
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