Association of G6PD with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemia.

Abstract

The genetic bases of the highly variable degrees of anaemia and haemolysis in persons with Hb SS are not fully known, but several studies have indicated that G6PD deficiency is not a factor. The G6PD(202A) and G6PD(376G) alleles and alpha-thalassaemia were determined by molecular genetic testing in 261 children and adolescents with Hb SS in a multicentre… (More)
DOI: 10.1111/j.1365-2141.2010.08215.x

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