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Combinations of three different forms of alpha-thalassemia in a large Indian family from Durban, South Africa: hematological observations.

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Hb natal or α2(minus Tyr-Arg)β2: a high oxygen affinity α chain variant with a deleted carboxy-terminus resulting from a TAC → TAA (Tyr→ terminating codon) mutation in codon α140

A. Kutlar, T. Huisman, J. B. Wilson, 1988 .