Molecular Characterization of the Factor IX Gene in 28 Iranian Hemophilia B Patients

نویسندگان
Zeinali, Sirous ID 1
Lak, Manijeh ID 2
Green, Peter ID 3
Karimipour, Morteza ID 4
Graham Tuddenham, Edward ID 5
Nafissi, Nafiseh ID 6

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چکیده

Background: Heterogeneous mutations in the human coagulation factor IX gene lead to an X-linked recessive bleeding disorder known as hemophilia B. The disease is distributed worldwide with no ethnic or geographical priority. Materials and Methods: The aim of this study was to characterize the factor IX gene mutations in 28 ...

کلیدواژه‌ها
hemophilia B, factor IX gene, mutation, iran