Molecular detection of some mutations of G6PD in a sample of Iraqi patients
This study was constructed to discuss an issue regarding Glucose 6 phosphate dehydrogenase deficiency enzyme, and the genetic disorder that leading to heamolysis anemia. A total of 50 blood samples were collected from different hospitals (Yarmook Hospital, Center Child hospital , AL Alweyaa , Medical City) beside to 20 sample as a control (healthy).These samples were vary in the deficiency of the enzyme from mild to chronic according to the test of G6PD. The period time of collection samples took about three months from March to June 2014.