APA (7th ed.) Citation

HM, V., M, V., JJ, S., G, R., J, O., M, W., . . . H, K. (2024). Exome variant prioritization in a large cohort of hearing-impaired individuals indicates IKZF2 to be associated with non-syndromic hearing loss and guides future research of unsolved cases. Human genetics, 143(11), 1379. https://doi.org/10.1007/s00439-024-02706-w

Chicago Style (17th ed.) Citation

HM, Velde, et al. "Exome Variant Prioritization in a Large Cohort of Hearing-impaired Individuals Indicates IKZF2 to Be Associated with Non-syndromic Hearing Loss and Guides Future Research of Unsolved Cases." Human Genetics 143, no. 11 (2024): 1379. https://doi.org/10.1007/s00439-024-02706-w.

MLA (9th ed.) Citation

HM, Velde, et al. "Exome Variant Prioritization in a Large Cohort of Hearing-impaired Individuals Indicates IKZF2 to Be Associated with Non-syndromic Hearing Loss and Guides Future Research of Unsolved Cases." Human Genetics, vol. 143, no. 11, 2024, p. 1379, https://doi.org/10.1007/s00439-024-02706-w.