1. Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred. Issue 1 (December 2016) Authors: Gradstein, Libe; Zolotushko, Jenny; Sergeev, Yuri; Lavy, Itay; Narkis, Ginat; Perez, Yonatan; Guigui, Sarah; Sharon, Dror; Banin, Eyal; Walter, Eyal; Lifshitz, Tova; Birk, Ohad Journal: BMC medical genetics Issue: Volume 17:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗