Prevalence of 3.7 and 4.2 deletions in Sudanese patients with red cells hypochromia and microcytosis
Alpha-thalassemia is a genetic disorder characterized by deletions of one or more α globin genes that result in deficient of α globin chains reducing haemoglobin concentration. The study aimed to screen 97 pat...
Source: BMC Research Notes - Category: Research Authors: Hussam Ali Osman, Muzamil Mahdi Abdel Hamid, Rahimah Binti Ahmad, Mohamed Saleem and Sana Altahir Abdallah Tags: Research note Source Type: research