Whole-exome sequencing identifies two novel mutations in KCNQ4 in individuals with nonsyndromic hearing loss.

MLA

Jung, Jinsei, et al. “Whole-Exome Sequencing Identifies Two Novel Mutations in KCNQ4 in Individuals with Nonsyndromic Hearing Loss.” Scientific Reports, vol. 8, no. 1, Nov. 2018, p. 16659. EBSCOhost, https://doi.org/10.1038/s41598-018-34876-9.

APA

Jung, J., Choi, H. B., Koh, Y. I., Rim, J. H., Choi, H. J., Kim, S. H., Lee, J. H., An, J., Kim, A., Lee, J. S., Joo, S. Y., Yu, S., Choi, J. Y., Kang, T. M., & Gee, H. Y. (2018). Whole-exome sequencing identifies two novel mutations in KCNQ4 in individuals with nonsyndromic hearing loss. Scientific Reports, 8(1), 16659. https://doi.org/10.1038/s41598-018-34876-9

Chicago

Jung, Jinsei, Hyun Been Choi, Young Ik Koh, John Hoon Rim, Hye Ji Choi, Sung Huhn Kim, Jae Hyun Lee, et al. 2018. “Whole-Exome Sequencing Identifies Two Novel Mutations in KCNQ4 in Individuals with Nonsyndromic Hearing Loss.” Scientific Reports 8 (1): 16659. doi:10.1038/s41598-018-34876-9.