Nalaganje...
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-...
Shranjeno v:
| izdano v: | Ann Saudi Med |
|---|---|
| Main Authors: | , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
King Faisal Specialist Hospital and Research Centre
2012
|
| Teme: | |
| Online dostop: | 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 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|