APA (7th ed.) Citation

S, C., SM, v. L., DC, W., J, N., P, F., D, B., . . . AE, V. (2023). A mutation in ATP11A causes autosomal-dominant auditory neuropathy type 2. Human molecular genetics, 32(7), 1083. https://doi.org/10.1093/hmg/ddac267

Chicago Style (17th ed.) Citation

S, Chepurwar, et al. "A Mutation in ATP11A Causes Autosomal-dominant Auditory Neuropathy Type 2." Human Molecular Genetics 32, no. 7 (2023): 1083. https://doi.org/10.1093/hmg/ddac267.

MLA (9th ed.) Citation

S, Chepurwar, et al. "A Mutation in ATP11A Causes Autosomal-dominant Auditory Neuropathy Type 2." Human Molecular Genetics, vol. 32, no. 7, 2023, p. 1083, https://doi.org/10.1093/hmg/ddac267.