Multi-Omics Analysis in β-Thalassemia Using an <i>HBB</i> Gene-Knockout Human Erythroid Progenitor Cell Model
β-thalassemia is a hematologic disease that may be associated with significant morbidity and mortality. Increased expression of <i>HBG1/2</i> can ameliorate the severity of β-thalassemia. Compared to the unaffected population, some β-thalassemia patients display elevated <i>HBG1/2&...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-03-01
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Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/1422-0067/23/5/2807 |