Now showing items 1-3 of 3
?-thalassemia mutations in the iranian kurdish population of kurdistan and west azerbaijan provinces
The aim of this study was to investigate the prevalence and spectrum of ?-thalassemia (?-thal) mutations in the population of Sunni Muslim Kurds in western Iran and to set up a prenatal diagnostic laboratory. Sixty unrelated ...
Homozygosity for a Rare β0-Thalassemia Mutation [Frameshift Codons 25/26 (+T)] Causes β-Thalassemia Intermedia in an Iranian Family
The severity of ?-thalassemia (?-thal) is remarkable for its variability in different populations, even in different patients. We studied a family from Azerbaijan Province, Northwestern Iran, who had a rare ?0-thal mutation, ...
Molecular spectrum of ?-thalassemia mutations in Northwestern Iran
?-Thalassemia (?-thal) is a hereditary autosomal disorder with decreased or absent ?-globin chain synthesis. This study was designed to identify the common and rare ?-thal mutations in the Azerbaijan provinces, Northwestern ...