Article

Prevalence of 3.7 and 4.2 Deletions in Sudanese Patients with Red Cells Hypochromia and Microcytosis

2020-01-30

Abstract excerpt

<title>Abstract</title> <p>Objective: 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 patients with microcytosis and hypochromasia for the 3.7 and 4.2 alpha thalassemia deletion mutations. <h4>Results:</h4> Out of 97 patients screened, only 7 were carriers f...

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Literature Corpus work: b655cdc4-f1c8-5a1a-8686-4cf6a83ee8dd
DOI: 10.21203/rs.2.20530/v2

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