Associated Papers
Five new F10 variants in hereditary factor x deficiency detected by high-throughput sequencing.
Pastoret C et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2023
Analysis of 180 Genetic Variants in a New Interactive FX Variant Database Reveals Novel Insights into FX Deficiency.
Harris VA et al.
Th Open : Companion Journal to Thrombosis and Haemostasis, 2021
Management of a hemispherotomy for Rasmussen encephalitis in a patient with mild factor 10 deficiency and low von Willebrand factor levels.
Dargan C et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2021
Molecular mechanism of a novel Ser362Asn mutation causing inherited FX deficiency in a Chinese family.
Zhang X et al.
International Journal of Hematology, 2020
Genotyping of five Pakistani patients with severe inherited factor X deficiency: identification of two novel mutations.
Borhany M et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2018
Congenital coagulation factor X deficiency: Genetic analysis of five patients and functional characterization of mutant factor X proteins.
Nagaya S et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2018
Molecular pathology of rare bleeding disorders (RBDs) in India: a systematic review.
Kulkarni BP et al.
Plos One, 2014
Molecular basis of factor X deficiency cases from India.
Mota L et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2010
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