APA (7th ed.) Citation

F, A., A, M., IA, A., AM, S., F, A., Q, A., . . . M, U. (2025). A novel CLRN2 variant: Expanding the mutation spectrum and its critical role in isolated hearing impairment. Genes & genomics, 47(4), 417. https://doi.org/10.1007/s13258-024-01590-y

Chicago Style (17th ed.) Citation

F, Ahmad, Mahmood A, Almazni IA, Shakoori AM, Alhakami F, Alam Q, Ismail M, and Umair M. "A Novel CLRN2 Variant: Expanding the Mutation Spectrum and Its Critical Role in Isolated Hearing Impairment." Genes & Genomics 47, no. 4 (2025): 417. https://doi.org/10.1007/s13258-024-01590-y.

MLA (9th ed.) Citation

F, Ahmad, et al. "A Novel CLRN2 Variant: Expanding the Mutation Spectrum and Its Critical Role in Isolated Hearing Impairment." Genes & Genomics, vol. 47, no. 4, 2025, p. 417, https://doi.org/10.1007/s13258-024-01590-y.