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The XmnI polymorphic site 5’ to the gene G(γ) in a Brazilian patient with sickle cell anaemia – fetal haemoglobin concentration, haematology and clinical features
We report a 20-year-old female with sickle cell anaemia and with an HbF concentration of 15.8%. The patient was not using hydroxyurea and was not receiving regular blood transfusions. The patient never had chronic manifestations of sickle cell anaemia, only pain crises of a mild intensity. After lab...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Termedia Publishing House
2010
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3298355/ https://ncbi.nlm.nih.gov/pubmed/22419945 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5114/aoms.2010.17101 |
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