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Autosomal dominant diabetes arising from a Wolfram syndrome 1 mutation
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Common Variants in Maturity-Onset Diabetes of the Young Genes Contribute to Risk of Type 2 Diabetes in Finns
Association of Transcription Factor 7-Like 2 (TCF7L2) Variants With Type 2 Diabetes in a Finnish Sample
Common variants in the GDF5-UQCC region are associated with variation in human height
