APA (7th ed.) Citation

M, V., V, V., MA, G., W, B., M, M., P, V., & LJ, L. (2025). Nitisinone desensitization protocol, case report of hereditary Tyrosinemia type 1 with successful treatment and outcomes. Orphanet journal of rare diseases, 20(1), 332. https://doi.org/10.1186/s13023-025-03666-8

Chicago Style (17th ed.) Citation

M, Vallejo, Villarreal V, Guardiola MA, Bachiller W, Moreno M, Vargas P, and López LJ. "Nitisinone Desensitization Protocol, Case Report of Hereditary Tyrosinemia Type 1 with Successful Treatment and Outcomes." Orphanet Journal of Rare Diseases 20, no. 1 (2025): 332. https://doi.org/10.1186/s13023-025-03666-8.

MLA (9th ed.) Citation

M, Vallejo, et al. "Nitisinone Desensitization Protocol, Case Report of Hereditary Tyrosinemia Type 1 with Successful Treatment and Outcomes." Orphanet Journal of Rare Diseases, vol. 20, no. 1, 2025, p. 332, https://doi.org/10.1186/s13023-025-03666-8.