Hemophilia is an X-linked recessive genetic bleeding disorder that occurs in two major forms. Approximately 80% of patients with hemophilia have mutations in the factor VIII clotting-factor gene (hemophilia A), and approximately 20% have mutations in the factor IX clotting factor gene (hemophilia…
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Πέμπτη 7 Δεκεμβρίου 2017
Closing In on Treatment for Hemophilia B
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