Cite
DNAJC30 defect: a frequent cause of recessive Leber hereditary optic neuropathy and Leigh syndrome.
MLA
Stenton, Sarah L., et al. “DNAJC30 Defect: A Frequent Cause of Recessive Leber Hereditary Optic Neuropathy and Leigh Syndrome.” Brain: A Journal of Neurology, vol. 145, no. 5, May 2022, pp. 1624–31. EBSCOhost, https://doi.org/10.1093/brain/awac052.
APA
Stenton, S. L., Tesarova, M., Sheremet, N. L., Catarino, C. B., Carelli, V., Ciara, E., Curry, K., Engvall, M., Fleming, L. R., Freisinger, P., Iwanicka-Pronicka, K., Jurkiewicz, E., Klopstock, T., Koenig, M. K., Kolářová, H., Kousal, B., Krylova, T., Morgia, C. L., Nosková, L., & Piekutowska-Abramczuk, D. (2022). DNAJC30 defect: a frequent cause of recessive Leber hereditary optic neuropathy and Leigh syndrome. Brain: A Journal of Neurology, 145(5), 1624–1631. https://doi.org/10.1093/brain/awac052
Chicago
Stenton, Sarah L., Marketa Tesarova, Natalia L. Sheremet, Claudia B. Catarino, Valerio Carelli, Elżbieta Ciara, Kathryn Curry, et al. 2022. “DNAJC30 Defect: A Frequent Cause of Recessive Leber Hereditary Optic Neuropathy and Leigh Syndrome.” Brain: A Journal of Neurology 145 (5): 1624–31. doi:10.1093/brain/awac052.