Investigation of RFLP Haplotypes β- Globin Gene Cluster in Beta-Thalassemia Patients in Central Iran

Investigation of RFLP Haplotypes β- Globin Gene Cluster in Beta-Thalassemia Patients in Central Iran

Background: Beta-thalassemia is one of the most prevalent inherited blood diseases among Iranians. The aim of this study was to elucidate the chromosomal background of beta-thalassemia mutations in Esfahan province, Iran. Materials and Methods: In this study, we investigated three frequent mutations...

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Bibliographic Details
Main Authors: Zahra Sajadpoor, Zeinab Amini-Farsani, Majid Motovali-Bashi, Mitra Yadollahi, Farrokh Yadollahi
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2019-04-01
Series:International Journal of Hematology-Oncology and Stem Cell Research
Subjects:
Haplotype; Beta-thalassemia; c.315 1G>A; c.92 5G>C; c.93-21G>A
Online Access:https://ijhoscr.tums.ac.ir/index.php/ijhoscr/article/view/928

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