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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...
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| Päätekijät: | , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Hindawi Publishing Corporation
2010
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2873658/ https://ncbi.nlm.nih.gov/pubmed/20508726 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2010/938640 |
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