APA (7th ed.) Citation

Y, C., R, D., HC, K., SL, S., S, W., A, L., . . . N, W. (2024). De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders. MedRxiv : the preprint server for health sciences. https://doi.org/10.1101/2024.04.07.24305438

Chicago Style (17th ed.) Citation

Y, Chen, et al. "De Novo Variants in the Non-coding Spliceosomal SnRNA Gene RNU4-2 Are a Frequent Cause of Syndromic Neurodevelopmental Disorders." MedRxiv : The Preprint Server for Health Sciences 2024. https://doi.org/10.1101/2024.04.07.24305438.

MLA (9th ed.) Citation

Y, Chen, et al. "De Novo Variants in the Non-coding Spliceosomal SnRNA Gene RNU4-2 Are a Frequent Cause of Syndromic Neurodevelopmental Disorders." MedRxiv : The Preprint Server for Health Sciences, 2024, https://doi.org/10.1101/2024.04.07.24305438.