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Epigenetic Insights and Potential Modifiers as Therapeutic Targets in β–Thalassemia
Thalassemia, an inherited quantitative globin disorder, consists of two types, α– and β–thalassemia. β–thalassemia is a heterogeneous disease that can be asymptomatic, mild, or even severe. Considerable research has focused on investigating its underlying etiology. These studies found that DNA hypom...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8158146/ https://www.ncbi.nlm.nih.gov/pubmed/34070036 http://dx.doi.org/10.3390/biom11050755 |