APA (7th ed.) Citation

Z, N., A, S., S, N., H, K., F, K., & MA, T. (2024). Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsia. BMC medical genomics, 17(1), 173. https://doi.org/10.1186/s12920-024-01942-3

Chicago Style (17th ed.) Citation

Z, Nouri, Sarmadi A, Narrei S, Kianersi H, Kianersi F, and Tabatabaiefar MA. "Clinical Characterizations and Molecular Genetic Study of Two Co-segregating Variants in PDZD7 and PDE6C Genes Leading Simultaneously to Non-syndromic Hearing Loss and Achromatopsia." BMC Medical Genomics 17, no. 1 (2024): 173. https://doi.org/10.1186/s12920-024-01942-3.

MLA (9th ed.) Citation

Z, Nouri, et al. "Clinical Characterizations and Molecular Genetic Study of Two Co-segregating Variants in PDZD7 and PDE6C Genes Leading Simultaneously to Non-syndromic Hearing Loss and Achromatopsia." BMC Medical Genomics, vol. 17, no. 1, 2024, p. 173, https://doi.org/10.1186/s12920-024-01942-3.