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β-Thalassemia hijacking ineffective erythropoietin and iron overload: Two case reports and a review of literature
Thalassemia is a rare, complex disease, representing a group of disorders of hemoglobin synthesis that are characterized by reduced synthesis of either the alpha-globin or β-globin chains of the hemoglobin molecule. Defective synthesis of β-globin resulting from a variety of molecular defects causes...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4121935/ https://www.ncbi.nlm.nih.gov/pubmed/25097435 http://dx.doi.org/10.4103/0976-9668.136245 |