1. NPHP1 gene deletion is a rare cause of Joubert syndrome related disorders. Issue 2 (2nd February 2005) Authors: Castori, M; Valente, E M; Donati, M A; Salvi, S; Fazzi, E; Procopio, E; Galluccio, T; Emma, F; Dallapiccola, B; Bertini, E Other Names: group-author. Journal: Journal of medical genetics Issue: Volume 42:Issue 2(2005) Page Start: e9 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗