Salkie M L, Gordon P A, Rigal W M, Lam H, Wilson J B, Headlee M E, Huisman T H
Hemoglobin. 1982;6(3):223-31. doi: 10.3109/03630268208991698.
An Indian family is described in which the father has a delta chain abnormal hemoglobin which is the result of a mutation of the delta gene in cis to a beta-thalassemia heterozygosity. The abnormality concerns a substitution of the Asp residue in position 99 (G1) by an Asn residue. A similar substitution has been found in the beta chain of Hb Kempsey (alpha 2 beta 2 99 Asp replaced by Asn). The observed abnormality results in a greatly increased oxygen affinity of this newly discovered Hb A2 variant.