刊物主题:Internal Medicine; Metabolic Diseases; Human Physiology;
出版者:Springer Berlin Heidelberg
ISSN:1432-0428
卷排序:60
文摘
Aims/hypothesisGenome-wide association studies (GWASs) have identified many common type 2 diabetes-associated variants, mostly at the intronic or intergenic regions. Recent advancements of exome-array genotyping platforms have opened up a novel means for detecting the associations of low-frequency or rare coding variants with type 2 diabetes. We conducted an exomechip association analysis to identify additional type 2 diabetes susceptibility variants in the Chinese population.