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

Viana, Marcos Borato

De novo alpha 2 hemoglobin gene (HBA2) mutation in a child with hemoglobin M Iwate and symptomatic methemoglobinemia since birth. [electronic resource] - Revista brasileira de hematologia e hemoterapia - 230-4 p. digital

Publication Type: Journal Article

1516-8484

10.1016/j.bjhh.2014.03.020 doi