The study of relationships between β-globin gene mutations in β-thalassaemia patients, in response to hydroxyurea treatment

The study of relationships between β-globin gene mutations in β-thalassaemia patients, in response to hydroxyurea treatment

AbstractBackground and Purpose: β-thalassaemia is the most frequent inherited disorder in the world, especially in Iran and Mazandaran Province. It is caused by mulation in β-globin gene on chromosome 11 with more than 150 different mulations causing β-thalassaemia, has been identified in the β-glob...

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Bibliographic Details
Main Authors: S. Zeinali, H. Karami, A. Banihashemi, F. Mojtahedzadeh, A. Aliasgharian, M. Kosarian, H. Akhavan Niaki, M.B. Hashemi Soteh
Format: Article
Language:English
Published: Mazandaran University of Medical Sciences 2008-01-01
Series:Journal of Mazandaran University of Medical Sciences
Subjects:
β-thalassaemia
Hydroxyurea
Mutation
Online Access:http://www.mazums.ac.ir/index.php?digital_library&do=downloadPdf&sid=609

Internet

http://www.mazums.ac.ir/index.php?digital_library&do=downloadPdf&sid=609

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