Associated Papers
Analysis of 272 Genetic Variants in the Upgraded Interactive FXI Web Database Reveals New Insights into FXI Deficiency.
Harris VA et al.
Th Open : Companion Journal to Thrombosis and Haemostasis, 2021
Genetic analysis in Factor XI deficient patients from central China: identification of one novel and seven recurrent mutations.
Liu H et al.
Gene, 2015
Antigenic peptide molecular recognition by the DRB1-DQB1 haplotype modulates multiple sclerosis susceptibility.
Kumar A et al.
Molecular Biosystems, 2014
Molecular characterization of FXI deficiency.
Berber E
Clinical and Applied Thrombosis/hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/hemostasis, 2011
Characterization of seven novel mutations causing factor XI deficiency.
Zucker M et al.
Haematologica, 2007
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