Liao, C., Ashley, N., Morten, K., Phadwal, K., Williams, A., Fearnley, I., . . . Poulton, J. (2012). O02 Dysregulated mitophagy and mitochondrial transport in severe dominant optic atrophy due to OPA1 mutations. Neuromuscular Disorders, 22(s1), S3. https://doi.org/10.1016/S0960-8966(12)70003-2
Chicago Style (17th ed.) CitationLiao, C., et al. "O02 Dysregulated Mitophagy and Mitochondrial Transport in Severe Dominant Optic Atrophy Due to OPA1 Mutations." Neuromuscular Disorders 22, no. s1 (2012): S3. https://doi.org/10.1016/S0960-8966(12)70003-2.
MLA (9th ed.) CitationLiao, C., et al. "O02 Dysregulated Mitophagy and Mitochondrial Transport in Severe Dominant Optic Atrophy Due to OPA1 Mutations." Neuromuscular Disorders, vol. 22, no. s1, 2012, p. S3, https://doi.org/10.1016/S0960-8966(12)70003-2.