APA (7th ed.) Citation

Jiang, Z., Mao, K., Wang, B., Zhu, H., Liu, J., Lang, R., . . . Zhang, Y. (2025). Deciphering TCOF1 mutations in Chinese Treacher Collins syndrome patients: Insights into pathogenesis and transcriptional disruption. Orphanet Journal of Rare Diseases, 20(1), 1. https://doi.org/10.1186/s13023-024-03508-z

Chicago Style (17th ed.) Citation

Jiang, Zhuoyuan, et al. "Deciphering TCOF1 Mutations in Chinese Treacher Collins Syndrome Patients: Insights into Pathogenesis and Transcriptional Disruption." Orphanet Journal of Rare Diseases 20, no. 1 (2025): 1. https://doi.org/10.1186/s13023-024-03508-z.

MLA (9th ed.) Citation

Jiang, Zhuoyuan, et al. "Deciphering TCOF1 Mutations in Chinese Treacher Collins Syndrome Patients: Insights into Pathogenesis and Transcriptional Disruption." Orphanet Journal of Rare Diseases, vol. 20, no. 1, 2025, p. 1, https://doi.org/10.1186/s13023-024-03508-z.