1. D-DEMØ, a distinct phenotype caused by ATP1A3 mutations. (October 2020) Authors: Prange, Lyndsey; Pratt, Milton; Herman, Kristin; Schiffmann, Raphael; Mueller, David M.; McLean, Melissa; Mendez, Mary Moya; Walley, Nicole; Heinzen, Erin L.; Goldstein, David; Shashi, Vandana; Hunanyan, Arsen; Pagadala, Vijay; Mikati, Mohamad A. Journal: Neurology Issue: Volume 6:Number 5(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗