A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation. - Liguori, Maria; La Russa, Antonella; Manna, Ida; Andreoli, Virginia; Caracciolo, Manuela; Spadafora, Patrizia; Cittadella, Rita; Quattrone, Aldo (Journal of Neurology, 2008)