Novel heterozygous mutation c.662_663insG compound with IVS7-2A>G mutation in SLC26A4 gene in a Chinese family with Pendred syndrome.

MLA

Chen, Kaitian, et al. “Novel Heterozygous Mutation c.662_663insG Compound with IVS7-2A>G Mutation in SLC26A4 Gene in a Chinese Family with Pendred Syndrome.” International Journal of Pediatric Otorhinolaryngology, vol. 76, no. 11, Nov. 2012, pp. 1633–36. EBSCOhost, https://doi.org/10.1016/j.ijporl.2012.07.035.

APA

Chen, K., Zhou, W., Zong, L., Liu, M., Du, J., & Jiang, H. (2012). Novel heterozygous mutation c.662_663insG compound with IVS7-2A>G mutation in SLC26A4 gene in a Chinese family with Pendred syndrome. International Journal of Pediatric Otorhinolaryngology, 76(11), 1633–1636. https://doi.org/10.1016/j.ijporl.2012.07.035

Chicago

Chen, Kaitian, Wei Zhou, Ling Zong, Min Liu, Jintao Du, and Hongyan Jiang. 2012. “Novel Heterozygous Mutation c.662_663insG Compound with IVS7-2A>G Mutation in SLC26A4 Gene in a Chinese Family with Pendred Syndrome.” International Journal of Pediatric Otorhinolaryngology 76 (11): 1633–36. doi:10.1016/j.ijporl.2012.07.035.