APA (7th ed.) Citation

Jiang, H., Niu, Y., Qu, L., Huang, X., Zhu, X., & Tang, G. (2018). A novel compound heterozygous mutation in the GJB2 gene is associated with non-syndromic hearing loss in a Chinese family. BioScience Trends, 12(5), 470. https://doi.org/10.5582/bst.2018.01156

Chicago Style (17th ed.) Citation

Jiang, Haiou, Youya Niu, Lingfeng Qu, Xueshuang Huang, Xinlong Zhu, and Genyun Tang. "A Novel Compound Heterozygous Mutation in the GJB2 Gene Is Associated with Non-syndromic Hearing Loss in a Chinese Family." BioScience Trends 12, no. 5 (2018): 470. https://doi.org/10.5582/bst.2018.01156.

MLA (9th ed.) Citation

Jiang, Haiou, et al. "A Novel Compound Heterozygous Mutation in the GJB2 Gene Is Associated with Non-syndromic Hearing Loss in a Chinese Family." BioScience Trends, vol. 12, no. 5, 2018, p. 470, https://doi.org/10.5582/bst.2018.01156.