... containing NBD2 is mutated in persistent hyperinsulinaemic hypoglycaemia of infancy. The disease is autosomal recessive and is characterized by profound neonatal hypoglycaemia and inappropriate ... 28079–28082.34. Matsuoka, T., Matsushita, K., Katayama, Y. , Fujita, A. ,Inageda, K., Tanemoto, M., Inanobe, A. , Yamashita, S.,Matsuzawa, Y. & Kurachi, Y. (2000) C-terminal tails of sulfo-nylurea receptors ... hyperinsulinaemichypoglycaemia of infancy is an hereditary disease char-acterized by inappropriately high levels of insulin release and hypoglycaemia in children at birth. It is hypothesizedthat deletion of the...