A novel exon 1 mutation in a patient with atypical Lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit

Authors: Annesi, G; Sofia, V; Gambardella, A; Candiano, ICC; Spadafora, P; Annesi, F; Cutuli, N; De Marco, EV; Civitelli, D; Carrideo, S; Tarantino, P; Barone, R; Zappia, M; Quattrone, A
Years: 2004
Source Title: EPILEPSIA
Doi: 10.1111/j.0013-9580.2004.33203.x
Venue: LiCryL @ Rende (CS)