Molecular Analysis of β-Globin Mutations Among β-Thalassemia Patients in Hamadan

Background: β-Thalassemia (βT) is one of the most common genetic diseases. The specific mutation profile of that region can be identified by determining the specific mutations of each region and ethnicity. Objectives: This study investigated the β-globin mutations in patients with βT in Hamadan....

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Auteurs principaux: Fatemeh Ramezani, Fatemeh Bahreini, Hossein Ranjbar, Ali Reza Soltanian
Format: article
Langue:EN
Publié: Hamadan University of Medical Sciences 2021
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Accès en ligne:https://doaj.org/article/6346fb6290624dfebacc8ae8ea076898
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