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β-Thalassemia: HiJAKing Ineffective Erythropoiesis and Iron Overload
β-thalassemia encompasses a group of monogenic diseases that have in common defective synthesis of β-globin. The defects involved are extremely heterogeneous and give rise to a large phenotypic spectrum, with patients that are almost asymptomatic to cases in which regular blood transfusions are requ...
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Hindawi Publishing Corporation
2010
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873658/ https://www.ncbi.nlm.nih.gov/pubmed/20508726 http://dx.doi.org/10.1155/2010/938640 |