Tetra-Primer ARMS PCR Optimization for Detection of IVS-II-I (G-A) and FSC 8/9 InsG Mutations in β-Thalassemia Major Patients in Isfahan Population

Background: β -thalassemia, a monogenic autosomal recessive disorder, is prevalent in Middle East, particularly in Iran. In Iran, near to 20 mutations in the β-globin gene are introduced as common mutations with varying incidence frequencies in each city. Therefore, detection and screening for coupl...

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Main Authors: Samaneh Hajihoseini (Author), Majid Motovali-Bashi (Author), Mohammad Amin Honardoost (Author), Nader Alerasool (Author)
Formato: Livro
Publicado em: Tehran University of Medical Sciences, 2015-03-01T00:00:00Z.
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