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Hemoglobin
international journal for hemoglobin research
Volume 1, 1976 - Issue 2
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Original Article

Hb-Alberta or α2β2 (101(G3) GLU→GLY), a New High-Oxygen-Affinity Hemoglobin Variant Causing Erythrocytosis

, , , , , , , & show all
Pages 183-194 | Published online: 07 Jul 2009
 

Abstract

Hb-Alberta has been found in a 51 year old Caucasian male with erythrocytosis. The substitution in this variant involves the glutamyl residue in position lOl(G3) of the β chain which is replaced by a glycyl residue. Hb-Alberta accounts for about 45% in the heterozygote, and readily forms hybrid tetramers with other hemoglobins. The oxygen affinity of Hb-Alberta is greatly increased, its Bohr effect reduced, and its subunit interaction greatly diminished.

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