Detection of IVSII-1 Mutation of Beta Globin Gene in Carriers of Thalassemia Minor Using High-Resolution Melting Analysis
Background: Beta-thalassemia is one of the most common autosomal recessive disorders in the world population caused by more than 200 different mutations in the beta-globin chain. It is clinically classified as minor, intermediate and major. Beta-thalassemia is the most common monogenic disease in th...
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Vesnu Publications
2016-02-01
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doaj-bc9c33ccc707451f99d799fc9667b1902020-11-25T01:33:43ZfasVesnu Publications مجله دانشکده پزشکی اصفهان1027-75951735-854X2016-02-0133363217921862099Detection of IVSII-1 Mutation of Beta Globin Gene in Carriers of Thalassemia Minor Using High-Resolution Melting AnalysisFatemeh Akhondi0Mojtaba Emadi-Baygi1Mansour Salehi2Parvaneh Nikpour3Department of Genetics, School of Basic Sciences, Shahrekord University, Shahrekord, IranAssistant Professor, Department of Genetics, School of Basic Sciences AND Research Institute of Biotechnology, Shahrekord University, Shahrekord, IranAssociate Professor, Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, IranAssistant Professor, Applied Physiology Research Center AND Child Growth and Development Research Center, Research Institute for Primordial Prevention of Non-communicable Disease AND Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, IranBackground: Beta-thalassemia is one of the most common autosomal recessive disorders in the world population caused by more than 200 different mutations in the beta-globin chain. It is clinically classified as minor, intermediate and major. Beta-thalassemia is the most common monogenic disease in the Mediterranean countries, Middle East, Indian Subcontinent, and Southeast Asia and one of the widespread hereditary disorders in Iran. Among differenthttp://jims.mui.ac.ir/index.php/jims/article/view/5567Beta thalassemia minorIVSII-1(G/A)High-resolution melting (HRM)Normalized plotDifference plot |
collection |
DOAJ |
language |
fas |
format |
Article |
sources |
DOAJ |
author |
Fatemeh Akhondi Mojtaba Emadi-Baygi Mansour Salehi Parvaneh Nikpour |
spellingShingle |
Fatemeh Akhondi Mojtaba Emadi-Baygi Mansour Salehi Parvaneh Nikpour Detection of IVSII-1 Mutation of Beta Globin Gene in Carriers of Thalassemia Minor Using High-Resolution Melting Analysis مجله دانشکده پزشکی اصفهان Beta thalassemia minor IVSII-1(G/A) High-resolution melting (HRM) Normalized plot Difference plot |
author_facet |
Fatemeh Akhondi Mojtaba Emadi-Baygi Mansour Salehi Parvaneh Nikpour |
author_sort |
Fatemeh Akhondi |
title |
Detection of IVSII-1 Mutation of Beta Globin Gene in Carriers of Thalassemia Minor Using High-Resolution Melting Analysis |
title_short |
Detection of IVSII-1 Mutation of Beta Globin Gene in Carriers of Thalassemia Minor Using High-Resolution Melting Analysis |
title_full |
Detection of IVSII-1 Mutation of Beta Globin Gene in Carriers of Thalassemia Minor Using High-Resolution Melting Analysis |
title_fullStr |
Detection of IVSII-1 Mutation of Beta Globin Gene in Carriers of Thalassemia Minor Using High-Resolution Melting Analysis |
title_full_unstemmed |
Detection of IVSII-1 Mutation of Beta Globin Gene in Carriers of Thalassemia Minor Using High-Resolution Melting Analysis |
title_sort |
detection of ivsii-1 mutation of beta globin gene in carriers of thalassemia minor using high-resolution melting analysis |
publisher |
Vesnu Publications |
series |
مجله دانشکده پزشکی اصفهان |
issn |
1027-7595 1735-854X |
publishDate |
2016-02-01 |
description |
Background: Beta-thalassemia is one of the most common autosomal recessive disorders in the world population caused by more than 200 different mutations in the beta-globin chain. It is clinically classified as minor, intermediate and major. Beta-thalassemia is the most common monogenic disease in the Mediterranean countries, Middle East, Indian Subcontinent, and Southeast Asia and one of the widespread hereditary disorders in Iran. Among different |
topic |
Beta thalassemia minor IVSII-1(G/A) High-resolution melting (HRM) Normalized plot Difference plot |
url |
http://jims.mui.ac.ir/index.php/jims/article/view/5567 |
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