Carregant...
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-...
Guardat en:
| Publicat a: | Ann Saudi Med |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
King Faisal Specialist Hospital and Research Centre
2012
|
| Matèries: | |
| Accés en línia: | 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 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|