Heterogeneity in disease severity in a family with a novel G68V GCK activating mutation causing persistent hyperinsulinaemic hypoglycaemia of infancy
Version of Record online: 1 NOV 2007
Volume 24, Issue 12, pages 1393–1399, December 2007
How to Cite
Wabitsch, M., Lahr, G., Van de Bunt, M., Marchant, C., Lindner, M., Von Puttkamer, J., Fenneberg, A., Debatin, K. M., Klein, R., Ellard, S., Clark, A. and Gloyn, A. L. (2007), Heterogeneity in disease severity in a family with a novel G68V GCK activating mutation causing persistent hyperinsulinaemic hypoglycaemia of infancy. Diabetic Medicine, 24: 1393–1399. doi: 10.1111/j.1464-5491.2007.02285.x
- Issue online: 26 NOV 2007
- Version of Record online: 1 NOV 2007
- Accepted 19 June 2007
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