1. Linkage analysis and exome sequencing identify a novel mutation in KCTD7 in patients with progressive myoclonus epilepsy with ataxia. Issue 9 (24th July 2014) Authors: Farhan, Sali M. K.; Murphy, Lisa M.; Robinson, John F.; Wang, Jian; Siu, Victoria M.; Rupar, C. Anthony; Prasad, Asuri N.; FORGE Canada Consortium; Hegele, Robert A. Journal: Epilepsia Issue: Volume 55:Issue 9(2014:Sep.) Page Start: e106 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗