APA (7th ed.) Citation

E, C., N, D., E, C., O, A., F, Z., I, L., . . . S, S. (2023). A homozygous variant in CHMP3 is associated with complex hereditary spastic paraplegia. Journal of medical genetics, 60(3), 233. https://doi.org/10.1136/jmedgenet-2022-108508

Chicago Style (17th ed.) Citation

E, Cohen-Barak, et al. "A Homozygous Variant in CHMP3 Is Associated with Complex Hereditary Spastic Paraplegia." Journal of Medical Genetics 60, no. 3 (2023): 233. https://doi.org/10.1136/jmedgenet-2022-108508.

MLA (9th ed.) Citation

E, Cohen-Barak, et al. "A Homozygous Variant in CHMP3 Is Associated with Complex Hereditary Spastic Paraplegia." Journal of Medical Genetics, vol. 60, no. 3, 2023, p. 233, https://doi.org/10.1136/jmedgenet-2022-108508.