Bileşik Heterozigot SEC23B Gen Mutasyonu Olan Konjenital Diseritropetik Anemi Tip 2 Olgusu
Journal Title: Turkish Journal of Hematology - Year 2015, Vol 32, Issue 3
Abstract
Authors and Affiliations
Fatih Demircioğlu, Mustafa Erkoçoğlu, Mervan Bekdaş, Sevil Göksügür, Semra Büyükkorkmaz, Seher Açar
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Use of a High-Purity Factor X Concentrate in Turkish Subjects with Hereditary Factor X Deficiency: Post Hoc Cohort Subanalysis of a Phase 3 Study
Hereditary factor X (FX) deficiency is a rare bleeding disorder more prevalent in countries with high rates of consanguineous marriage. In a prospective, open-label, multicenter phase 3 study, 25 IU/kg plasmaderived fact...
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