APA (7th ed.) Citation

CA, T., ML, E., M, N., R, M., & NM, E. (2025). Concurrent novel mutations in PAX3 and CFAP410 in a patient with Waardenburg syndrome type 1 associated with Retinitis Pigmentosa. Ophthalmic genetics, 46(3), 305. https://doi.org/10.1080/13816810.2025.2473972

Chicago Style (17th ed.) Citation

CA, Tawfik, Essawi ML, Nowara M, Mohsen R, and Elbagoury NM. "Concurrent Novel Mutations in PAX3 and CFAP410 in a Patient with Waardenburg Syndrome Type 1 Associated with Retinitis Pigmentosa." Ophthalmic Genetics 46, no. 3 (2025): 305. https://doi.org/10.1080/13816810.2025.2473972.

MLA (9th ed.) Citation

CA, Tawfik, et al. "Concurrent Novel Mutations in PAX3 and CFAP410 in a Patient with Waardenburg Syndrome Type 1 Associated with Retinitis Pigmentosa." Ophthalmic Genetics, vol. 46, no. 3, 2025, p. 305, https://doi.org/10.1080/13816810.2025.2473972.