APA (7th ed.) Citation

Zhao, X., Chi, H., Bai, Y., Lu, Y., Xiong, W., Kang, H., & Zhang, C. (2025). Analysis of clinical phenotypes and genotypes of congenital deafness caused by rare variants in GJB2. Frontiers in pediatrics, 13, 1514369. https://doi.org/10.3389/fped.2025.1514369

Chicago Style (17th ed.) Citation

Zhao, Xuxu, Huan Chi, Yan Bai, Yu Lu, Wenyu Xiong, Houyong Kang, and Cheng Zhang. "Analysis of Clinical Phenotypes and Genotypes of Congenital Deafness Caused by Rare Variants in GJB2." Frontiers in Pediatrics 13 (2025): 1514369. https://doi.org/10.3389/fped.2025.1514369.

MLA (9th ed.) Citation

Zhao, Xuxu, et al. "Analysis of Clinical Phenotypes and Genotypes of Congenital Deafness Caused by Rare Variants in GJB2." Frontiers in Pediatrics, vol. 13, 2025, p. 1514369, https://doi.org/10.3389/fped.2025.1514369.