1. Deep intronic KRIT1 mutation in a family with clinically silent multiple cerebral cavernous malformations. (20th December 2013) Authors: Riant, F.; Odent, S.; Cecillon, M.; Pasquier, L.; de Baracé, C.; Carney, M.P.; Tournier‐Lasserve, E. Journal: Clinical genetics Issue: Volume 86:Number 6(2014:Dec.) Page Start: 585 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. PRRT2 mutations and paroxysmal disorders. Issue 6 (9th February 2013) Authors: Méneret, A.; Gaudebout, C.; Riant, F.; Vidailhet, M.; Depienne, C.; Roze, E. Journal: European journal of neurology Issue: Volume 20:Issue 6(2013:Jun.) Page Start: 872 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗