1. De novo loss of function mutations in KIAA2022 are associated with epilepsy and neurodevelopmental delay in females. Issue 5 (29th September 2016) Authors: Webster, R.; Cho, M.T.; Retterer, K.; Millan, F.; Nowak, C.; Douglas, J.; Ahmad, A.; Raymond, G.V.; Johnson, M.R.; Pujol, A.; Begtrup, A.; McKnight, D.; Devinsky, O.; Chung, W.K. Journal: Clinical genetics Issue: Volume 91:Issue 5(2017) Page Start: 756 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗