Phenotypic heterogeneity in a family with a novel activating glucokinase (GCK) mutation (G68V) causing familial persistent hyperinsulinaemic hypoglycaemia of infancy

Detalles Bibliográficos
Autores principales:	Gloyn, A, Marchant, C, Linder, M, von Puttkamer, J, Wasser, A, Clark, A, Ellard, S, Lahr, G, Wabitsch, M
Formato:	Journal article
Publicado:	2007

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