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

Introduction: 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 mutatio...

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Pubblicato in:Int J Hematol Oncol Stem Cell Res
Autori principali: Sajadpour, Zahra, Amini-Farsani, Zeinab, Motovali-Bashi, Majid, Yadollahi, Mitra, Yadollahi, Farrokh
Natura: Artigo
Lingua:Inglês
Pubblicazione: Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center 2019
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6660478/
https://ncbi.nlm.nih.gov/pubmed/31372199
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