APA (7th ed.) Citation

Trinchillo, A., Valente, V., Esposito, M., Migliaccio, M., Iovino, A., Picciocchi, M., . . . Criscuolo, C. (2024). Expanding SPG18 clinical spectrum: Autosomal dominant mutation causes complicated hereditary spastic paraplegia in a large family. Neurological sciences, 45(9), 4373-4381. https://doi.org/10.1007/s10072-024-07500-0

Chicago Style (17th ed.) Citation

Trinchillo, Assunta, et al. "Expanding SPG18 Clinical Spectrum: Autosomal Dominant Mutation Causes Complicated Hereditary Spastic Paraplegia in a Large Family." Neurological Sciences 45, no. 9 (2024): 4373-4381. https://doi.org/10.1007/s10072-024-07500-0.

MLA (9th ed.) Citation

Trinchillo, Assunta, et al. "Expanding SPG18 Clinical Spectrum: Autosomal Dominant Mutation Causes Complicated Hereditary Spastic Paraplegia in a Large Family." Neurological Sciences, vol. 45, no. 9, 2024, pp. 4373-4381, https://doi.org/10.1007/s10072-024-07500-0.