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Epigenetic inactivation of ERF reactivates γ-globin expression in β-thalassemia
The fetal-to-adult hemoglobin switch is regulated in a developmental stage-specific manner and reactivation of fetal hemoglobin (HbF) has therapeutic implications for treatment of β-thalassemia and sickle cell anemia, two major global health problems. Although significant progress has been made in o...
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| Pubblicato in: | Am J Hum Genet |
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| Autori principali: | , , , , , , , , , , , , , , , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Elsevier
2021
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8059375/ https://ncbi.nlm.nih.gov/pubmed/33735615 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2021.03.005 |
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