1. Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia. Issue 1 (11th May 2016) Authors: Barresi, S.; Niceta, M.; Alfieri, P.; Brankovic, V.; Piccini, G.; Bruselles, A.; Barone, M.R.; Cusmai, R.; Tartaglia, M.; Bertini, E.; Zanni, G. Journal: Clinical genetics Issue: Volume 91:Issue 1(2017) Page Start: 86 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗