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
Characterization of hereditary factor XI deficiency in Taiwanese patients: identification of three novel and two common mutations.
Lin HY et al.
International Journal of Hematology, 2020
Gene variants in four pedigrees with hereditary coagulation factor XI deficiency and one novel mutation identification.
Lin F et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2020
[Phenotype and Genotype Analysis in Two Pedigrees with Hereditary Coagulation Factor Ⅺ Deficiency].
Weng MS et al.
Sichuan Da Xue Xue Bao. Yi Xue Ban = Journal of Sichuan University. Medical Science Edition, 2020
Clinical manifestations and mutation spectrum of 57 subjects with congenital factor XI deficiency in China.
Shao Y et al.
Blood Cells, Molecules & Diseases, 2016
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