Liguori, M., La Russa, A., Manna, I., Andreoli, V., Caracciolo, M., Spadafora, P., . . . Quattrone, A. (2008). A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation. Journal of Neurology, 255(1), 127. https://doi.org/10.1007/s00415-008-0571-x
Chicago Style (17th ed.) CitationLiguori, Maria, Antonella La Russa, Ida Manna, Virginia Andreoli, Manuela Caracciolo, Patrizia Spadafora, Rita Cittadella, and Aldo Quattrone. "A Phenotypic Variation of Dominant Optic Atrophy and Deafness (ADOAD) Due to a Novel OPA1 Mutation." Journal of Neurology 255, no. 1 (2008): 127. https://doi.org/10.1007/s00415-008-0571-x.
MLA (9th ed.) CitationLiguori, Maria, et al. "A Phenotypic Variation of Dominant Optic Atrophy and Deafness (ADOAD) Due to a Novel OPA1 Mutation." Journal of Neurology, vol. 255, no. 1, 2008, p. 127, https://doi.org/10.1007/s00415-008-0571-x.