Hemoglobin Athens‐Georgia [α2 β2 40(C6)Arg→Lys] in association with β0‐thalassemia in Tunisia

We describe an Hb Athens‐Georgia (Hb A‐Ga)/β0‐thalassemia compound heterozygosity, found in a Tunisian patient. Oxygen binding studies of red cell suspensions of this patient, containing approximately 95% Hb A‐Ga, revealed an almost normal oxygen affinity. Nevertheless, dilute solutions of Hb A‐Ga s...

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Veröffentlicht in:	American journal of hematology 1989-10, Vol.32 (2), p.117-122
Hauptverfasser:	Mrad, A., Kister, J., Feo, C., Poyart, C., Kastally, R., Blibech, R., Galacteros, F., Wajcman, H.
Format:	Artikel
Sprache:	eng
Schlagworte:	Anemias. Hemoglobinopathies Biological and medical sciences Diseases of red blood cells ektacytometric studies Hb Waco Hematologic and hematopoietic diseases Medical sciences oxygen binding
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