APA (7th ed.) Citation

Granjo, P., Pascoal, C., Gallego, D., Francisco, R., Jaeken, J., Moors, T., . . . dos Reis Ferreira, V. (2024). Mapping the diagnostic odyssey of congenital disorders of glycosylation (CDG): Insights from the community. Orphanet Journal of Rare Diseases, 19(1), 1. https://doi.org/10.1186/s13023-024-03389-2

Chicago Style (17th ed.) Citation

Granjo, Pedro, et al. "Mapping the Diagnostic Odyssey of Congenital Disorders of Glycosylation (CDG): Insights from the Community." Orphanet Journal of Rare Diseases 19, no. 1 (2024): 1. https://doi.org/10.1186/s13023-024-03389-2.

MLA (9th ed.) Citation

Granjo, Pedro, et al. "Mapping the Diagnostic Odyssey of Congenital Disorders of Glycosylation (CDG): Insights from the Community." Orphanet Journal of Rare Diseases, vol. 19, no. 1, 2024, p. 1, https://doi.org/10.1186/s13023-024-03389-2.