Associated Papers
Hb Dapu (HBA2: c.52G > T): A Novel Nondeletional α-Thalassemia Mutation.
Yang Y et al.
Hemoglobin, 2016
Mutation near the binding interfaces at α-hemoglobin stabilizing protein is highly pathogenic.
Borgio JF et al.
American Journal of Translational Research, 2016
Mutations on the α2-Globin Gene That May Trigger α(+)-Thalassemia.
Farashi S et al.
Hemoglobin, 2015
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