APA (7th ed.) Citation

P, W., N, S., Y, X., Z, T., B, M., R, G., . . . J, M. (2025). FOXK2 in skeletal muscle development: A new pathogenic gene for congenital myopathy with ptosis. EMBO molecular medicine, 17(7), 1599. https://doi.org/10.1038/s44321-025-00247-x

Chicago Style (17th ed.) Citation

P, Wu, et al. "FOXK2 in Skeletal Muscle Development: A New Pathogenic Gene for Congenital Myopathy with Ptosis." EMBO Molecular Medicine 17, no. 7 (2025): 1599. https://doi.org/10.1038/s44321-025-00247-x.

MLA (9th ed.) Citation

P, Wu, et al. "FOXK2 in Skeletal Muscle Development: A New Pathogenic Gene for Congenital Myopathy with Ptosis." EMBO Molecular Medicine, vol. 17, no. 7, 2025, p. 1599, https://doi.org/10.1038/s44321-025-00247-x.