Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations

Mutations at the gene encoding wolframin (WFS1) cause Wolfram syndrome, a rare neurological condition. Associations between single nucleotide polymorphisms (SNPs) at WFS1 and type 2 diabetes have recently been reported. Thus, our aim was to replicate those associations in a northern Swedish case-con...

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Veröffentlicht in:	Diabetologia 2008-03, Vol.51 (3), p.523-523
Hauptverfasser:	Franks, P. W., Rolandsson, O., Debenham, S. L., Fawcett, K. A., Payne, F., Dina, C., Froguel, P., Mohlke, K. L., Willer, C., Olsson, T., Wareham, N. J., Hallmans, G., Barroso, I., Sandhu, M. S.
Format:	Artikel
Sprache:	eng
Schlagworte:	Erratum Human Physiology Internal Medicine Medicine Medicine & Public Health Metabolic Diseases
Online-Zugang:	Volltext
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