Variation of DNA Repair Genes APE1 and RAD18 in β-Thalassemia Patients

Background: In the last decade, beta-thalassemia (β-thalassemia) has been recorded in high percentages among the Iraqi population and this disorder has a deficiency in β-globin chains causing striking heterogeneity of molecular disorder. The study subjects’ characteristics showed nonsignificant diff...

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Bibliographic Details
Main Authors: Nawras Najah Jawad, Mona N. Al-Terehi
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2024-12-01
Series:Medical Journal of Babylon
Subjects:
Online Access:https://doi.org/10.4103/MJBL.MJBL_1747_23
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