(2016). Molecular characterization of β-Thalassemia patients in Wasit province. Alustath, 9(2), 70-77.
. "Molecular characterization of β-Thalassemia patients in Wasit province". Alustath, 9, 2, 2016, 70-77.
(2016). 'Molecular characterization of β-Thalassemia patients in Wasit province', Alustath, 9(2), pp. 70-77.
Molecular characterization of β-Thalassemia patients in Wasit province. Alustath, 2016; 9(2): 70-77.

Molecular characterization of β-Thalassemia patients in Wasit province

Journal Of Wassit For Science & Medicine
Article 1, Volume 9, Issue 2, August 2016, Pages 70-77
Abstract
Abstract
Background: Hemoglobin-associated disorder is a different group of recessive genetic diseases. Which consist of the structural hemoglobin variants and the thalassemia.Aim of the study: to characterize the spectrum of beta globin gene mutations in patients with beta- thalassemia who are registered in thalassemia centers, Wasit, Iraq using PCR - based DNA diagnostic techniques.
Patients and methods: The genomic DNA was extracted from 106 Iraqi patients with β-thalassemia major and intermedia from unrelated families and (50) healthy numbers as control were collected from Al-Kut Hospital, in Wasit province, to detect mutation using PCR - based DNA diagnostic techniques. .
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