Smits, J. J., de Bruijn, S. E., Lanting, C. P., Oostrik, J., O’Gorman, L., Mantere, T., . . . Kremer, H. (2022). Correction to: 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), 991. https://doi.org/10.1007/s00439-021-02377-x
Chicago-Zitierstil (17. Ausg.)Smits, Jeroen J., et al. "Correction to: 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): 991. https://doi.org/10.1007/s00439-021-02377-x.
MLA-Zitierstil (9. Ausg.)Smits, Jeroen J., et al. "Correction to: 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, p. 991, https://doi.org/10.1007/s00439-021-02377-x.