1. Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly. (5th February 2015) Authors: Paciorkowski, Alex R.; McDaniel, Sharon S.; Jansen, Laura A.; Tully, Hannah; Tuttle, Emily; Ghoneim, Dalia H.; Tupal, Srinivasan; Gunter, Sonya A.; Vasta, Valeria; Zhang, Qing; Tran, Thao; Liu, Yi B.; Ozelius, Laurie J.; Brashear, Allison; Sweadner, Kathleen J.; Dobyns, William B.; Hahn, Sihoun Journal: Epilepsia Issue: Volume 56:issue 3(2015:Mar.) Page Start: 422 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗