Analysis of β/α Globin Ratio by Using Relative qRT-PCR for Diagnosis of Beta-Thalassemia Carriers

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Comparisons between RT-PCR, real-time PCR, and in vitro globin chain synthesis by α/β ratio calculation for diagnosis of α- from β-thalassemia carriers.

BACKGROUND Thalassemia, which may be due to point mutations, translocations, and deletions involving the α or βglobin gene, is the most prevalent single gene disorder in Iran.This study aims to calculate the α/β ratio in normal cases, α- and β-thalassemia carriers by RT-PCR, real-time PCR, and in vitro globin chain synthesis (GCS) in order to establish the most accurate technique to distinguish...

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Comparisons between RT-PCR, Real-time PCR, and In Vitro Globin Chain Synthesis by a/b Ratio Calculation for Diagnosis of a- from b-thalassemia Carriers

T halassemia syndromes are the most prevalent autosomal recessive single gene disorders in Iran.1,2 Interactions of different types of hemoglobinopathies can lead to thalassemia syndromes with a variety of phenotypes that range from asymptomatic to severe anemia. The diversity of thalassemia phenotypes depends on the amount of imbalances created between and non-globin chains.3,4 In normal eryth...

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ژورنال

عنوان ژورنال: Journal of Clinical Laboratory Analysis

سال: 2013

ISSN: 0887-8013

DOI: 10.1002/jcla.21594