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HARVARD Citation

    Azimi, A. et al. (2020). Severe α-Thalassemia Due to Compound Heterozygosity for Hb Adana (α59 Gly>Asp) (HBA1: c.179G > A) and Codon 127 (A > T) (HBA2: c.382A > T) in an Iranian Family. Hemoglobin. pp. 139-142. [Online]. 
  
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