APA (7th ed.) Citation

F, I., S, T., N, Y., J, R., & S, L. (2023). Prolidase deficiency: A novel PEPD missense variant in exon 2. American journal of medical genetics. Part A, 191(5), 1388. https://doi.org/10.1002/ajmg.a.63137

Chicago Style (17th ed.) Citation

F, Ido, Tessier S, Yoder N, Ramzy J, and Longo S. "Prolidase Deficiency: A Novel PEPD Missense Variant in Exon 2." American Journal of Medical Genetics. Part A 191, no. 5 (2023): 1388. https://doi.org/10.1002/ajmg.a.63137.

MLA (9th ed.) Citation

F, Ido, et al. "Prolidase Deficiency: A Novel PEPD Missense Variant in Exon 2." American Journal of Medical Genetics. Part A, vol. 191, no. 5, 2023, p. 1388, https://doi.org/10.1002/ajmg.a.63137.