APA (7th ed.) Citation

K, H., A, S., Y, K., Y, A., H, A., M, Y., . . . T, M. (2026). PHOX2B deletion in congenital central hypoventilation syndrome: Is this sufficient for pathogenesis? Journal of human genetics, 71(4), 203. https://doi.org/10.1038/s10038-025-01429-8

Chicago Style (17th ed.) Citation

K, Hayasaka, et al. "PHOX2B Deletion in Congenital Central Hypoventilation Syndrome: Is This Sufficient for Pathogenesis?" Journal of Human Genetics 71, no. 4 (2026): 203. https://doi.org/10.1038/s10038-025-01429-8.

MLA (9th ed.) Citation

K, Hayasaka, et al. "PHOX2B Deletion in Congenital Central Hypoventilation Syndrome: Is This Sufficient for Pathogenesis?" Journal of Human Genetics, vol. 71, no. 4, 2026, p. 203, https://doi.org/10.1038/s10038-025-01429-8.