Mutation analysis of common GJB2, SCL26A4 and 12S rRNA genes among 380 deafness patients in northern China.

MLA

Pan, Jing, et al. “Mutation Analysis of Common GJB2, SCL26A4 and 12S RRNA Genes among 380 Deafness Patients in Northern China.” International Journal of Pediatric Otorhinolaryngology, vol. 98, July 2017, pp. 39–42. EBSCOhost, https://doi.org/10.1016/j.ijporl.2017.04.018.

APA

Pan, J., Xu, P., Tang, W., Cui, Z., Feng, M., & Wang, C. (2017). Mutation analysis of common GJB2, SCL26A4 and 12S rRNA genes among 380 deafness patients in northern China. International Journal of Pediatric Otorhinolaryngology, 98, 39–42. https://doi.org/10.1016/j.ijporl.2017.04.018

Chicago

Pan, Jing, Ping Xu, Weibo Tang, Zhongtao Cui, Miao Feng, and Chunying Wang. 2017. “Mutation Analysis of Common GJB2, SCL26A4 and 12S RRNA Genes among 380 Deafness Patients in Northern China.” International Journal of Pediatric Otorhinolaryngology 98 (July): 39–42. doi:10.1016/j.ijporl.2017.04.018.