APA (7th ed.) Citation

Klouwer, F. C., Roosendaal, S. D., Hollak, C. E. M., Langeveld, M., Poll-The, B. T., Sorge, A. J. v., . . . Engelen, M. (2024). Redefining the phenotype of alpha-methylacyl-CoA racemase (AMACR) deficiency. Orphanet Journal of Rare Diseases, 19(1), 1. https://doi.org/10.1186/s13023-024-03358-9

Chicago Style (17th ed.) Citation

Klouwer, Femke C.C., Stefan D. Roosendaal, Carla E. M. Hollak, Mirjam Langeveld, Bwee Tien Poll-The, Arlette J. van Sorge, Nicole I. Wolf, Marjo S. van der Knaap, and Marc Engelen. "Redefining the Phenotype of Alpha-methylacyl-CoA Racemase (AMACR) Deficiency." Orphanet Journal of Rare Diseases 19, no. 1 (2024): 1. https://doi.org/10.1186/s13023-024-03358-9.

MLA (9th ed.) Citation

Klouwer, Femke C.C., et al. "Redefining the Phenotype of Alpha-methylacyl-CoA Racemase (AMACR) Deficiency." Orphanet Journal of Rare Diseases, vol. 19, no. 1, 2024, p. 1, https://doi.org/10.1186/s13023-024-03358-9.