HIGHLIGHTS
- who: Jason Flannick from the Finland Finland have published the research work: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls, in the Journal: (JOURNAL) of 31/05/2017
- how: Each variant was tested for association with T2D in the sequenced individuals and to increase power most were tested in larger numbers of individuals (>80% of low-frequency coding variants in ~82 K Europeans via the exome chip and ~90% of low-frequency non-coding variants in ~44 K Europeans via genotype imputation). Statistics of the 2657 individuals ultimately included . . .
If you want to have access to all the content you need to log in!
Thanks :)
If you don't have an account, you can create one here.