APA (7th ed.) Citation

A, C., A, R., E, D., B, G., I, B., I, M., . . . LA, P. (2022). FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects. Genetics in medicine : official journal of the American College of Medical Genetics, 24(12), 2475. https://doi.org/10.1016/j.gim.2022.09.002

Chicago Style (17th ed.) Citation

A, Cospain, et al. "FOSL2 Truncating Variants in the Last Exon Cause a Neurodevelopmental Disorder with Scalp and Enamel Defects." Genetics in Medicine : Official Journal of the American College of Medical Genetics 24, no. 12 (2022): 2475. https://doi.org/10.1016/j.gim.2022.09.002.

MLA (9th ed.) Citation

A, Cospain, et al. "FOSL2 Truncating Variants in the Last Exon Cause a Neurodevelopmental Disorder with Scalp and Enamel Defects." Genetics in Medicine : Official Journal of the American College of Medical Genetics, vol. 24, no. 12, 2022, p. 2475, https://doi.org/10.1016/j.gim.2022.09.002.