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Hemoglobin H

Hemoglobin H disease is a type of alpha thalassemia caused by impaired production of three of the four alpha globins, coded by genes HBA1 and HBA2. Hemoglobin H disease is a type of alpha thalassemia caused by impaired production of three of the four alpha globins, coded by genes HBA1 and HBA2.

[ "Globin", "Hemolytic anemia", "Thalassemia", "Hemoglobinopathy", "Genotype", "Acquired hemoglobin H disease", "Hemoglobin H Constant Spring", "Hemoglobin H inclusions" ]
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