Biallelic rare 17 bp deletion mutation (HBB:c.380_396 del TGCAGGCTGCCTATCAG) in a transfusion depended form of thalassemia. [electronic resource]

By: Contributor(s): Producer: 20201105Description: 2719-2722 p. digitalISSN:
  • 1432-0584
Subject(s): Online resources: In: Annals of hematology vol. 99
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Publication Type: Case Reports; Letter

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