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Control of fetal hemoglobin: new insights emerging from genomics and clinical implications
Increased levels of fetal hemoglobin (HbF, α(2)γ(2)) are of no consequence in healthy adults, but confer major clinical benefits in patients with sickle cell anemia (SCA) and β thalassemia, diseases that represent major public health problems. Inter-individual HbF variation is largely genetically co...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2758709/ https://ncbi.nlm.nih.gov/pubmed/19808799 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddp401 |
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