APA (7th ed.) Citation

Antonicka, H., Weraarpachai, W., Szigety, K. M., Kopajtich, R., Gibson, J. B., Van Hove, J. L., . . . Shoubridge, E. A. (2025). Bi-allelic mutations in FASTKD5 are associated with cytochrome c oxidase deficiency and early- to late-onset Leigh syndrome. American journal of human genetics, 112(7), 1699-1710. https://doi.org/10.1016/j.ajhg.2025.05.007

Chicago Style (17th ed.) Citation

Antonicka, Hana, et al. "Bi-allelic Mutations in FASTKD5 Are Associated with Cytochrome C Oxidase Deficiency and Early- to Late-onset Leigh Syndrome." American Journal of Human Genetics 112, no. 7 (2025): 1699-1710. https://doi.org/10.1016/j.ajhg.2025.05.007.

MLA (9th ed.) Citation

Antonicka, Hana, et al. "Bi-allelic Mutations in FASTKD5 Are Associated with Cytochrome C Oxidase Deficiency and Early- to Late-onset Leigh Syndrome." American Journal of Human Genetics, vol. 112, no. 7, 2025, pp. 1699-1710, https://doi.org/10.1016/j.ajhg.2025.05.007.