Verrigni, D., Di Nottia, M., Ardissone, A., Baruffini, E., Nasca, A., Legati, A., . . . Bertini, E. (2019). Clinical‐genetic features and peculiar muscle histopathology in infantile DNM1L‐related mitochondrial epileptic encephalopathy. Human mutation, 40(5), 601-618.
Chicago Style (17th ed.) CitationVerrigni, Daniela, et al. "Clinical‐genetic Features and Peculiar Muscle Histopathology in Infantile DNM1L‐related Mitochondrial Epileptic Encephalopathy." Human Mutation 40, no. 5 (2019): 601-618.
MLA (8th ed.) CitationVerrigni, Daniela, et al. "Clinical‐genetic Features and Peculiar Muscle Histopathology in Infantile DNM1L‐related Mitochondrial Epileptic Encephalopathy." Human Mutation, vol. 40, no. 5, 2019, pp. 601-618.
Warning: These citations may not always be 100% accurate.
Visit our Citation Styles guide for help on properly citing sources.
Visit our Citation Styles guide for help on properly citing sources.