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Sickle cell anaemia (SCA) results from a single mutation in the β globin gene. It is seldom symptomatic in the first semester of life. We analysed the expression pattern of 9 adhesion molecules on red blood cells, in a cohort of 54 SCA and 17 non-SCA very young infants of comparable age (median 144days, 81–196). Haemoglobin F (HbF) level was unsurprisingly elevated in SCA infants (41.2%±11.2) and...
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