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2.
Haematologica ; 91(4): 570-1, 2006 Apr.
Article in English | MEDLINE | ID: mdl-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.


Subject(s)
Hemoglobins, Abnormal/genetics , Mutation, Missense , alpha-Thalassemia/genetics , Adult , Family Health , Female , Globins/genetics , Humans , Turkey
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