1. NOVEL CONE DYSTROPHY WITH CENTRAL ELLIPSOID ZONE LOSS ASSOCIATED WITH HUMAN RETINAL FASCIN GENE (FSCN2) MUTATION. (2018) Authors: Gui, Wei; Nusinowitz, Steven; Sarraf, David Journal: Retinal cases & brief reports Issue: Volume 12(2018)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗