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Homozygosity for a Rare β 0 -Thalassemia Mutation [Frameshift Codons 25/26 (+T)] Causes β-Thalassemia Intermedia in an Iranian Family
Haghi, Mehdi, Hosseinpour Feizi, Abbas A., Harteveld, Cornelis L., Pouladi, Nasser, Hosseinpour Feizi, Mohammad A.Volume:
33
Language:
english
Journal:
Hemoglobin
DOI:
10.1080/03630260802683377
Date:
January, 2009
File:
PDF, 169 KB
english, 2009