Francisco, R., Brasil, S., Poejo, J., Jaeken, J., Pascoal, C., Videira, P. A., & dos Reis Ferreira, V. (2023). Congenital disorders of glycosylation (CDG): State of the art in 2022. Orphanet Journal of Rare Diseases, 18(1), 1. https://doi.org/10.1186/s13023-023-02879-z
Chicago Style (17th ed.) CitationFrancisco, Rita, Sandra Brasil, Joana Poejo, Jaak Jaeken, Carlota Pascoal, Paula A. Videira, and Vanessa dos Reis Ferreira. "Congenital Disorders of Glycosylation (CDG): State of the Art in 2022." Orphanet Journal of Rare Diseases 18, no. 1 (2023): 1. https://doi.org/10.1186/s13023-023-02879-z.
MLA (9th ed.) CitationFrancisco, Rita, et al. "Congenital Disorders of Glycosylation (CDG): State of the Art in 2022." Orphanet Journal of Rare Diseases, vol. 18, no. 1, 2023, p. 1, https://doi.org/10.1186/s13023-023-02879-z.