APA (7th ed.) Citation

Vallortigara, J., Greenfield, J., Hunt, B., Hoffman, D., Reinhard, C., Graessner, H., . . . Giunti, P. (2023). Patient pathways for rare diseases in Europe: Ataxia as an example. Orphanet journal of rare diseases, 18(1), 1-10. https://doi.org/10.1186/s13023-023-02907-y

Chicago Style (17th ed.) Citation

Vallortigara, Julie, et al. "Patient Pathways for Rare Diseases in Europe: Ataxia as an Example." Orphanet Journal of Rare Diseases 18, no. 1 (2023): 1-10. https://doi.org/10.1186/s13023-023-02907-y.

MLA (9th ed.) Citation

Vallortigara, Julie, et al. "Patient Pathways for Rare Diseases in Europe: Ataxia as an Example." Orphanet Journal of Rare Diseases, vol. 18, no. 1, 2023, pp. 1-10, https://doi.org/10.1186/s13023-023-02907-y.