1. Neurodevelopmental models of transcription factor 4 deficiency converge on a common ion channel as a potential therapeutic target for Pitt Hopkins syndrome. Issue 1 (1st January 2016) Authors: Rannals, Matthew D.; Page, Stephanie Cerceo; Campbell, Morganne N.; Gallo, Ryan A.; Mayfield, Brent; Maher, Brady J. Journal: Rare diseases Issue: Volume 4:Issue 1(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗