Heterogeneity in disease severity in a family with a novel G68V GCK activating mutation causing persistent hyperinsulinaemic hypoglycaemia of infancy. (Diabetic medicine : a journal of the British Diabetic Association, 2007)

(untitled) - Wabitsch, M; Lahr, G; Van de Bunt, M; Marchant, C; Lindner, M; von Puttkamer, J; Fenneberg, A; Debatin, K; Klein, R; Ellard, S; Clark, A; Gloyn, A