APA (7th ed.) Citation

A, K., C, S., C, E., L, H., E, S., S, S., . . . J, M. (2025). Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability. American journal of human genetics, 112(12), 2943. https://doi.org/10.1016/j.ajhg.2025.10.014

Chicago Style (17th ed.) Citation

A, Kröll-Hermi, et al. "Bi-allelic PRMT9 Loss-of-function Variants Cause a Syndromic Form of Intellectual Disability." American Journal of Human Genetics 112, no. 12 (2025): 2943. https://doi.org/10.1016/j.ajhg.2025.10.014.

MLA (9th ed.) Citation

A, Kröll-Hermi, et al. "Bi-allelic PRMT9 Loss-of-function Variants Cause a Syndromic Form of Intellectual Disability." American Journal of Human Genetics, vol. 112, no. 12, 2025, p. 2943, https://doi.org/10.1016/j.ajhg.2025.10.014.