APA (7th ed.) Citation

P, B., S, B., N, P., E, A., G, D., D, T., . . . V, S. (2022). Genotype-phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders. Orphanet journal of rare diseases, 17(1), 286. https://doi.org/10.1186/s13023-022-02415-5

Chicago Style (17th ed.) Citation

P, Borgia, et al. "Genotype-phenotype Correlations and Disease Mechanisms in PEX13-related Zellweger Spectrum Disorders." Orphanet Journal of Rare Diseases 17, no. 1 (2022): 286. https://doi.org/10.1186/s13023-022-02415-5.

MLA (9th ed.) Citation

P, Borgia, et al. "Genotype-phenotype Correlations and Disease Mechanisms in PEX13-related Zellweger Spectrum Disorders." Orphanet Journal of Rare Diseases, vol. 17, no. 1, 2022, p. 286, https://doi.org/10.1186/s13023-022-02415-5.