HIGHLIGHTS
- who: Zoe Schmilovich et al. from the CNVs between cases with ASD and unselected individuals from the general population (n u2248, ) and replicate the findings in UKMcGill University have published the article: Copy-Number Variants in The Contactin-5 Gene Are a Potential Risk Factor for Autism Spectrum Disorder, in the Journal: (JOURNAL)
- what: Analysis, the authors identified an enrichment of intronic CNTN5 deletion in ASD compared to an unselected control population. Taken together, this study characterizes CNTN5 CNVs as inherited rare frequency variants in ASD. The authors show that CNTN5 CNVs are not fully . . .
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.