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Prevalence of Xmnl Gγ polymorphism in Egyptian patients with β-thalassemia major
BACKGROUND AND OBJECTIVES: β-thalassemia results from a deficiency of β-globin chains leading to an excess in α globin chains resulting in hypochromic microcytic red cells, ineffective erythropoiesis and hemolytic anemia. It is a result of a decline of HbF synthesis during the first year of life. F-...
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| Yayımlandı: | Ann Saudi Med |
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| Asıl Yazarlar: | , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
King Faisal Specialist Hospital and Research Centre
2012
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6080985/ https://ncbi.nlm.nih.gov/pubmed/22871617 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5144/0256-4947.2012.487 |
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