De novo alpha 2 hemoglobin gene (HBA2) mutation in a child with hemoglobin M Iwate and symptomatic methemoglobinemia since birth. [electronic resource]

By: Contributor(s): Producer: 20140717Description: 230-4 p. digitalISSN:
  • 1516-8484
Online resources: In: Revista brasileira de hematologia e hemoterapia vol. 36
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Publication Type: Journal Article

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