APA (7th ed.) Citation

Pintilie, S. R., Fodor, A., Bembea, M., Petchesi, C. D., Grad, S., Damian, L., & Vulturar, R. (2021). A rare but treatable inborn error of metabolism: Arginine glycine amidinotransferase (AGAT) deficiency. Romanian Journal of Pediatrics / Revista Romana de Pediatrie, 70(3), 186. https://doi.org/10.37897/RJP.2021.3.4

Chicago Style (17th ed.) Citation

Pintilie, Sebastian Romeo, Adriana Fodor, Marius Bembea, Codruța Diana Petchesi, Simona Grad, Laura Damian, and Romana Vulturar. "A Rare but Treatable Inborn Error of Metabolism: Arginine Glycine Amidinotransferase (AGAT) Deficiency." Romanian Journal of Pediatrics / Revista Romana De Pediatrie 70, no. 3 (2021): 186. https://doi.org/10.37897/RJP.2021.3.4.

MLA (9th ed.) Citation

Pintilie, Sebastian Romeo, et al. "A Rare but Treatable Inborn Error of Metabolism: Arginine Glycine Amidinotransferase (AGAT) Deficiency." Romanian Journal of Pediatrics / Revista Romana De Pediatrie, vol. 70, no. 3, 2021, p. 186, https://doi.org/10.37897/RJP.2021.3.4.