Table 1
Mutations found in patients with persistent hyperinsulinaemic hypoglycaemia of infancy (PHHI) within the SUR1 and KIR6.2 genes
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Tm, putative transmembrane domain (according to Swiss-ProtQ09428); NBD, nucleotide binding domain; ND, no data available; M2 region, one of two potential transmembrane spanning domains; nt nucleotide; bp base pairs.
