APA (7th ed.) Citation

Smits, J. J., de Bruijn, S. E., Lanting, C. P., Oostrik, J., O’Gorman, L., Mantere, T., . . . Kremer, H. (2022). Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant. Human genetics, 141(3-4), 465-484. https://doi.org/10.1007/s00439-021-02336-6

Chicago Style (17th ed.) Citation

Smits, Jeroen J., et al. "Exploring the Missing Heritability in Subjects with Hearing Loss, Enlarged Vestibular Aqueducts, and a Single or No Pathogenic SLC26A4 Variant." Human Genetics 141, no. 3-4 (2022): 465-484. https://doi.org/10.1007/s00439-021-02336-6.

MLA (9th ed.) Citation

Smits, Jeroen J., et al. "Exploring the Missing Heritability in Subjects with Hearing Loss, Enlarged Vestibular Aqueducts, and a Single or No Pathogenic SLC26A4 Variant." Human Genetics, vol. 141, no. 3-4, 2022, pp. 465-484, https://doi.org/10.1007/s00439-021-02336-6.