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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 ...