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
Diagnosis, clinical manifestations and management of rare bleeding disorders in Iran.
Dorgalaleh A et al.
Hematology (amsterdam, Netherlands), 2017
Factor XI deficiency in Southern Iran: identification of a novel missense mutation.
Karimi M et al.
Annals of Hematology, 2009
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