Abstract
In β-thalassaemia translation of haemoglobin β-chain mRNA appears to be normal. This suggests that defective regulation of mRNA production is probably responsible for the reduced rate of β-chain synthesis in this disorder.
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CLEGG, J., WEATHERALL, D., NA-NAKORN, S. et al. Haemoglobin Synthesis in β-Thalassaemia. Nature 220, 664–668 (1968). https://doi.org/10.1038/220664a0
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DOI: https://doi.org/10.1038/220664a0
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