Introduction: Hemophilia B is an X-linked recessive genetic disease caused by mutations in the coagulation Factor IX gene. Mutations in the Factor IX gene result in dysfunction or deficiency of coagulation factor of IX.
P Dorri, A Karimi , S Vallian boroujeni
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Retracted: Long Intergenic Nonprotein Coding RNA 00174 Aggravates Lung Squamous Cell Carcinoma Progression via MicroRNA-185-5p/Nuclear Factor IX axis. [PDF]
International BR.
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Stable and durable factor IX levels in patients with hemophilia B over 3 years after etranacogene dezaparvovec gene therapy. [PDF]
von Drygalski A+13 more
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The mechanism underlying activation of factor IX by factor XIa.
D. Gailani+6 more
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Blood Coagulation Factor IX: Structure, Function, and Regulation. [PDF]
Ivanciu L, Camire RM.
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Post hoc longitudinal assessment of the efficacy and safety of recombinant factor IX Fc fusion protein in hemophilia B. [PDF]
Shapiro AD+16 more
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Characteristics and Treatment Patterns of Patients with Haemophilia B Receiving Recombinant Coagulation Factor IX. [PDF]
Park YS+16 more
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Differences in wild-type- and R338L-tenase complex formation are at the root of R338L-factor IX assay discrepancies. [PDF]
Foley JH+12 more
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Extravascular factor IX after gene therapy in hemophilia B, does it matter? [PDF]
Van Thillo Q, Hermans C.
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Long-term outcomes of prophylaxis with a recombinant factor VIII Fc or recombinant factor IX Fc in patients with hemophilia previously treated on demand. [PDF]
Álvarez-Román MT+7 more
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