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Sickle Cell Anemia with Malaria: A Rare Case Report
Sickle cell disease is the prototype of hereditary hemoglobinopathies, characterized by the production of structurally abnormal hemoglobin. Sickle cell anemia results from a point mutation that leads to substitution of valine for glutamic acid at the sixth position of the β globin chain. We report a...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer India
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3921335/ https://ncbi.nlm.nih.gov/pubmed/24554820 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-012-0181-8 |
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