APA (7th ed.) Citation

Chikhaoui, A., Kraoua, I., Calmels, N., Bouchoucha, S., Obringer, C., Zayoud, K., . . . Yacoub-Youssef, H. (2022). Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations. Orphanet Journal of Rare Diseases, 17(1), 1. https://doi.org/10.1186/s13023-022-02257-1

Chicago Style (17th ed.) Citation

Chikhaoui, Asma, et al. "Heterogeneous Clinical Features in Cockayne Syndrome Patients and Siblings Carrying the Same CSA Mutations." Orphanet Journal of Rare Diseases 17, no. 1 (2022): 1. https://doi.org/10.1186/s13023-022-02257-1.

MLA (9th ed.) Citation

Chikhaoui, Asma, et al. "Heterogeneous Clinical Features in Cockayne Syndrome Patients and Siblings Carrying the Same CSA Mutations." Orphanet Journal of Rare Diseases, vol. 17, no. 1, 2022, p. 1, https://doi.org/10.1186/s13023-022-02257-1.