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Case Reports in Genetics
Volume 2011, Article ID 768610, 3 pages
http://dx.doi.org/10.1155/2011/768610
Case Report

A De Novo Whole GCK Gene Deletion Not Detected by Gene Sequencing, in a Boy with Phenotypic GCK Insufficiency

1Department of Pediatric, Aarhus University Hospital, Skejby, 8200 Aarhus C, Denmark
2Department of Clinical Genetic, Aarhus University Hospital, Nørrebrogade, 8200 Aarhus C, Denmark
3Hagedorn Research Institute, 2820 Gentofte, Denmark
4Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health Sciences, University of Copenhagen, 1350 Copenhagen K, Denmark
5University of Aarhus, 8200 Aarhus C, Denmark
6Steno Diabetes Center, 2820 Gentofte, Denmark
7Faculty of Health Sciences, University of Southern Denmark, 5000 Odense C, Denmark

Received 13 July 2011; Accepted 18 August 2011

Academic Editors: A. Baumer, C.-W. Cheng, and C. Yapijakis

Copyright © 2011 N. H. Birkebæk et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

N. H. Birkebæk, J. S. Sørensen, J. Vikre-Jørgensen, P. K. A. Jensen, O. Pedersen, and T. Hansen, “A De Novo Whole GCK Gene Deletion Not Detected by Gene Sequencing, in a Boy with Phenotypic GCK Insufficiency,” Case Reports in Genetics, vol. 2011, Article ID 768610, 3 pages, 2011. https://doi.org/10.1155/2011/768610.