APA (7th ed.) Citation

C, J., T, B., D, W., M, S., E, S., A, P., . . . L, F. (2026). De novo heterozygous variants of the RSF1 gene are responsible for a syndromic neurodevelopmental disorder. European journal of human genetics : EJHG, 34(4), 554. https://doi.org/10.1038/s41431-026-02017-w

Chicago Style (17th ed.) Citation

C, Jost, et al. "De Novo Heterozygous Variants of the RSF1 Gene Are Responsible for a Syndromic Neurodevelopmental Disorder." European Journal of Human Genetics : EJHG 34, no. 4 (2026): 554. https://doi.org/10.1038/s41431-026-02017-w.

MLA (9th ed.) Citation

C, Jost, et al. "De Novo Heterozygous Variants of the RSF1 Gene Are Responsible for a Syndromic Neurodevelopmental Disorder." European Journal of Human Genetics : EJHG, vol. 34, no. 4, 2026, p. 554, https://doi.org/10.1038/s41431-026-02017-w.