APA (7th ed.) Citation

Y, S., HT, L., BJ, L., & J, H. (2023). Expanding SPG7 dominant optic atrophy phenotype: Infantile nystagmus and optic atrophy without spastic paraplegia. American journal of medical genetics. Part A, 191(2), 582. https://doi.org/10.1002/ajmg.a.63037

Chicago Style (17th ed.) Citation

Y, Seo, Lim HT, Lee BJ, and Han J. "Expanding SPG7 Dominant Optic Atrophy Phenotype: Infantile Nystagmus and Optic Atrophy Without Spastic Paraplegia." American Journal of Medical Genetics. Part A 191, no. 2 (2023): 582. https://doi.org/10.1002/ajmg.a.63037.

MLA (9th ed.) Citation

Y, Seo, et al. "Expanding SPG7 Dominant Optic Atrophy Phenotype: Infantile Nystagmus and Optic Atrophy Without Spastic Paraplegia." American Journal of Medical Genetics. Part A, vol. 191, no. 2, 2023, p. 582, https://doi.org/10.1002/ajmg.a.63037.