APA (7th ed.) Citation

G, F., V, B., E, T., R, W., & F, J. (2025). Transcriptomic profiling of unmethylated full mutation carriers implicates TET3 in FMR1 CGG repeat expansion methylation dynamics in fragile X syndrome. Journal of neurodevelopmental disorders, 17(1), 22. https://doi.org/10.1186/s11689-025-09609-5

Chicago Style (17th ed.) Citation

G, Farmiloe, Bejczy V, Tabolacci E, Willemsen R, and Jacobs F. "Transcriptomic Profiling of Unmethylated Full Mutation Carriers Implicates TET3 in FMR1 CGG Repeat Expansion Methylation Dynamics in Fragile X Syndrome." Journal of Neurodevelopmental Disorders 17, no. 1 (2025): 22. https://doi.org/10.1186/s11689-025-09609-5.

MLA (9th ed.) Citation

G, Farmiloe, et al. "Transcriptomic Profiling of Unmethylated Full Mutation Carriers Implicates TET3 in FMR1 CGG Repeat Expansion Methylation Dynamics in Fragile X Syndrome." Journal of Neurodevelopmental Disorders, vol. 17, no. 1, 2025, p. 22, https://doi.org/10.1186/s11689-025-09609-5.