1. Novel homozygous mutation in exon 5 of WFS1 gene in an Apulian family with mild phenotypic expression of Wolfram syndrome. (3rd October 2013) Authors: Piccinno, E.; Ortolani, F.; Vendemiale, M.; Tummolo, A.; Masciopinto, M.; Natale, M.P.; De Luca, A.; Agolini, E.; Aloi, C.; Salina, A.; D'Annunzio, G.; Fischetto, R.; Papadia, F. Journal: Clinical genetics Issue: Volume 86:Number 2(2014:Aug.) Page Start: 197 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗