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-...

Descripción completa

Detalles Bibliográficos
Autores principales: Tantawy, Azza AG, Andrawes, Nevine G., Ismaeil, Amany, Kamel, Solaf A., Emam, Wessam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: King Faisal Specialist Hospital and Research Centre 2012
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6080985/
https://www.ncbi.nlm.nih.gov/pubmed/22871617
http://dx.doi.org/10.5144/0256-4947.2012.487

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6080985/
https://www.ncbi.nlm.nih.gov/pubmed/22871617
http://dx.doi.org/10.5144/0256-4947.2012.487

Ejemplares similares