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- W2023962907 abstract "The structure, synthesis, genetic transmission, clinical associations and distribution of the elongated α-chain haemoglobin variants has been described. The data indicate that the most likely molecular basis for these common abnormal haemoglobins is a single base substitution in the α-chain termination codon. Because these variants are produced inefficiently they give rise to the clinical picture of α-thalassaemia. When these findings are taken together with recent work regarding the molecular basis for other forms of a-thalassaemia it is possible to build up a fairly complete picture of the molecular pathology of the α-thalassaemias." @default.
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- W2023962907 date "1975-08-07" @default.
- W2023962907 modified "2023-09-26" @default.
- W2023962907 title "The α-chain-termination mutants and their relation to the α-thalassaemias" @default.
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- W2023962907 doi "https://doi.org/10.1098/rstb.1975.0061" @default.
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