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Analysis of Intron 1 Inversion at F8 Gene in Severe Hemophilia A Patients by Inverse Shifting-PCR Referred from Isfahan Seyedolshohada Hospital

Background & Objectives: Hemophilia A is an X-linked recessive bleeding disorder , which is caused by several different abnormalities in Factor 8 gene . Intron 22 inversion is the main causative mutation in 45-50% of severe hemophilia A patients. Moreover intron 1 inversion is responsible for >5% of...

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Bibliografski detalji
Glavni autori: Narghes Roozafzay, Leila Kokabee, Syrous Zeinali, Morteza Karimipoor
Format: Artigo
Jezik:Persa
Izdano: Ardabil University of Medical Sciences 2013-04-01
Serija:Journal of Ardabil University of Medical Sciences
Teme:
Online pristup:http://jarums.arums.ac.ir/browse.php?a_code=A-10-27-106&slc_lang=en&sid=1
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