APA (7th ed.) Citation

J, P., A, T., V, C., G, D., C, R., J, S., . . . H, H. (2022). Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy. Genetics in medicine : official journal of the American College of Medical Genetics, 24(10), 2079. https://doi.org/10.1016/j.gim.2022.07.006

Chicago Style (17th ed.) Citation

J, Park, et al. "Heterozygous UCHL1 Loss-of-function Variants Cause a Neurodegenerative Disorder with Spasticity, Ataxia, Neuropathy, and Optic Atrophy." Genetics in Medicine : Official Journal of the American College of Medical Genetics 24, no. 10 (2022): 2079. https://doi.org/10.1016/j.gim.2022.07.006.

MLA (9th ed.) Citation

J, Park, et al. "Heterozygous UCHL1 Loss-of-function Variants Cause a Neurodegenerative Disorder with Spasticity, Ataxia, Neuropathy, and Optic Atrophy." Genetics in Medicine : Official Journal of the American College of Medical Genetics, vol. 24, no. 10, 2022, p. 2079, https://doi.org/10.1016/j.gim.2022.07.006.