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  • Title: Hb Bronovo, a new globin gene mutation at alpha2 103 (His->Leu) associated with an alpha thalassemia phenotype.
    Author: Harteveld CL, Steen G, Vlasveld LT, van Delft P, Giordano PC.
    Journal: Haematologica; 2006 Apr; 91(4):570-1. PubMed ID: 16533721.
    Abstract:
    Mild alpha-thalassemia, a common condition in many ethnic groups, presents with hematologic abnormalities almost identical to those found in iron deficiency. We report a new alpha globin chain variant associated with an alpha-thalassemia phenotype in two members of a Turkish family.
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