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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 couple...

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Detalles Bibliográficos
Autores principales: HAJIHOSEINI, Samaneh, MOTOVALI-BASHI, Majid, HONARDOOST, Mohammad Amin, ALERASOOL, Nader
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4402417/
https://www.ncbi.nlm.nih.gov/pubmed/25905082

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