1. Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1‐related disorders. (6th August 2014) Authors: Chaussenot, A.; Rouzier, C.; Quere, M.; Plutino, M.; Ait‐El‐Mkadem, S.; Bannwarth, S.; Barth, M.; Dollfus, H.; Charles, P.; Nicolino, M.; Chabrol, B.; Vialettes, B.; Paquis‐Flucklinger, V. Journal: Clinical genetics Issue: Volume 87:Number 5(2015:May) Page Start: 430 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗