APA (7th ed.) Citation

RE, S., AE, P., D, B., K, J., BL, L., EH, J., . . . ME, P. (2025). Variants in CFAP410 cause a range of retinal and skeletal phenotypes. NPJ genomic medicine, 10(1), 32. https://doi.org/10.1038/s41525-025-00489-1

Chicago Style (17th ed.) Citation

RE, Schmidt, et al. "Variants in CFAP410 Cause a Range of Retinal and Skeletal Phenotypes." NPJ Genomic Medicine 10, no. 1 (2025): 32. https://doi.org/10.1038/s41525-025-00489-1.

MLA (9th ed.) Citation

RE, Schmidt, et al. "Variants in CFAP410 Cause a Range of Retinal and Skeletal Phenotypes." NPJ Genomic Medicine, vol. 10, no. 1, 2025, p. 32, https://doi.org/10.1038/s41525-025-00489-1.