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Erythropoiesis In Vitro—A Research and Therapeutic Tool in Thalassemia
Thalassemia (thal) is a hereditary chronic hemolytic anemia due to a partial or complete deficiency in the production of globin chains, in most cases, α or β, which compose, together with the iron-containing porphyrins (hemes), the hemoglobin molecules in red blood cells (RBC). The major clinical sy...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6947291/ https://www.ncbi.nlm.nih.gov/pubmed/31810354 http://dx.doi.org/10.3390/jcm8122124 |