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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Principais autores:	Narghes Roozafzay, Leila Kokabee, Syrous Zeinali, Morteza Karimipoor
Formato:	Artigo
Idioma:	Persa
Publicado em:	Ardabil University of Medical Sciences 2013-04-01
coleção:	Journal of Ardabil University of Medical Sciences
Assuntos:	Hemophilia A; Intron 1; Inverse Shifting-PCR; Inversion
Acesso em linha:	http://jarums.arums.ac.ir/browse.php?a_code=A-10-27-106&slc_lang=en&sid=1
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