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...

Fuld beskrivelse

Bibliografiske detaljer

Principais autores:	Narghes Roozafzay, Leila Kokabee, Syrous Zeinali, Morteza Karimipoor
Format:	Artigo
Sprog:	Persa
Udgivet:	Ardabil University of Medical Sciences 2013-04-01
Serier:	Journal of Ardabil University of Medical Sciences
Fag:	Hemophilia A; Intron 1; Inverse Shifting-PCR; Inversion
Online adgang:	http://jarums.arums.ac.ir/browse.php?a_code=A-10-27-106&slc_lang=en&sid=1
Tags:	Tilføj Tag Ingen Tags, Vær først til at tagge denne postø!