APA (7th ed.) Citation

RK, L., K, H., LN, W., C, J., T, A., MR, R., . . . C, G. (2026). FMR1 gene therapy restores translationally relevant phenotypes in a mouse model for fragile X syndrome. Gene therapy. https://doi.org/10.1038/s41434-026-00630-4

Chicago Style (17th ed.) Citation

RK, Lacher, et al. "FMR1 Gene Therapy Restores Translationally Relevant Phenotypes in a Mouse Model for Fragile X Syndrome." Gene Therapy 2026. https://doi.org/10.1038/s41434-026-00630-4.

MLA (9th ed.) Citation

RK, Lacher, et al. "FMR1 Gene Therapy Restores Translationally Relevant Phenotypes in a Mouse Model for Fragile X Syndrome." Gene Therapy, 2026, https://doi.org/10.1038/s41434-026-00630-4.