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Fetal hemoglobin reactivation and cell engineering in the treatment of sickle cell anemia
The natural history of severe hemoglobinopathies like sickle cell disease (SCD) is rather variable, depending on the circumstances, but the main influence on such variability is the level of fetal hemoglobin (HbF) in the patient’s red cells. It is well known that a significant HbF level is associate...
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| Main Authors: | , |
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| Format: | Artigo |
| Language: | Inglês |
| Published: |
Dove Medical Press
2011
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3262355/ https://ncbi.nlm.nih.gov/pubmed/22287860 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/JBM.S14942 |
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