APA (7th ed.) Citation

S, L., GH, S., SY, K., SS, J., S, J., S, C., . . . JH, C. (2025). Clinical utility of genome sequencing in rare diseases: Lessons from a single-center study of 1,452 Korean families. NPJ genomic medicine, 11(1), 2. https://doi.org/10.1038/s41525-025-00538-9

Chicago Style (17th ed.) Citation

S, Lee, et al. "Clinical Utility of Genome Sequencing in Rare Diseases: Lessons from a Single-center Study of 1,452 Korean Families." NPJ Genomic Medicine 11, no. 1 (2025): 2. https://doi.org/10.1038/s41525-025-00538-9.

MLA (9th ed.) Citation

S, Lee, et al. "Clinical Utility of Genome Sequencing in Rare Diseases: Lessons from a Single-center Study of 1,452 Korean Families." NPJ Genomic Medicine, vol. 11, no. 1, 2025, p. 2, https://doi.org/10.1038/s41525-025-00538-9.