HIGHLIGHTS
- who: Megan Y. Dennis and colleagues from the Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, United Kingdom, Genome Technology Branch, National Human Genome Research Institute have published the paper: A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene, in the Journal: (JOURNAL) of March/27,/2009
- what: The authors report additional genetic and functional characterization of the risk haplotype, specifically focusing on variants within the putative regulatory element(s) immediately upstream of KIAA0319. The study provides an empirical explanation for apparently contradictory complex trait-related genetic associations.
-
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.