Hb Bronovo, a new globin gene mutation at alpha2 103 (His->Leu) associated with an alpha thalassemia phenotype

Haematologica. 2006 Apr;91(4):570-1. Epub 2006 Mar 1.

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.

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Family Health
  • Female
  • Globins / genetics
  • Hemoglobins, Abnormal / genetics*
  • Humans
  • Mutation, Missense*
  • Turkey
  • alpha-Thalassemia / genetics*

Substances

  • Hemoglobins, Abnormal
  • hemoglobin Bronovo
  • Globins