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Beta cells, potassium channels, and insulin
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    https://doi.org/10.1136/adc.77.3.257

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      It seems that the term, nesidioblastosis, is out and persistent hyperinsulinaemic hypoglycaemia of infancy (PHHI) is in. In familial PHHI mutations have been found in the gene on the short arm of chromosome 11 which codes for a β …

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