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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Veröffentlicht in:Ann Saudi Med
Hauptverfasser: Tantawy, Azza AG, Andrawes, Nevine G., Ismaeil, Amany, Kamel, Solaf A., Emam, Wessam
Format: Artigo
Sprache:Inglês
Veröffentlicht: King Faisal Specialist Hospital and Research Centre 2012
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Original Article
Online Zugang: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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