Hb adana or α259(E8)Gly→Aspβ2, A severely unstable α1-globin variant, observed in combination with the -(α)20.5 KB α-thal-1 deletion in two Turkish patients

Author:

Çürük M. A.,Dimovski A. J.,Baysal E.,Gu L-H.,Kutlar F.,Molchanova T. P.,Webber B. B.,Altay Ç.,Gürgey A.,Huisman T. H. J.

Publisher

Wiley

Subject

Hematology

Reference31 articles.

1. α-Thalassemia and β-thalassemia in a turkish family

2. , , ,: Conventional isoelectric focusing and immobilized pH gradients for hemoglobin separation and identification. In (ed) : “The Hemoglobinopathies.” Edinburgh: Churchill Livingstone, 1986, p 47.

3. : “The Hemoglobinopathies Techniques of Identification.” New York: Marcel Dekker, 1977.

4. High-performance liquid chromatographic separation of human haemoglobins

5. Fetal hemoglobin in normal adults and ?-thalassemia heterozygotes

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