APA

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. & Gloyn A. L. (20080416). 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.

Chicago

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. 20080416. 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.

Harvard

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. (20080416). 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.

MLA

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. 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. 20080416.