Cite
A humanized murine model, demonstrating dominant progressive hearing loss caused by a novel KCNQ4 mutation (p.G228D) from a large Chinese family.
MLA
Cui, Chong, et al. “A Humanized Murine Model, Demonstrating Dominant Progressive Hearing Loss Caused by a Novel KCNQ4 Mutation (p.G228D) from a Large Chinese Family.” Clinical Genetics, vol. 102, no. 2, Aug. 2022, pp. 149–54. EBSCOhost, https://doi.org/10.1111/cge.14164.
APA
Cui, C., Zhang, L., Qian, F., Chen, Y., Huang, B., Wang, F., Wang, D., Lv, J., Wang, X., Yan, Z., Guo, L., Li, G.-L., Shu, Y., Liu, D., & Li, H. (2022). A humanized murine model, demonstrating dominant progressive hearing loss caused by a novel KCNQ4 mutation (p.G228D) from a large Chinese family. Clinical Genetics, 102(2), 149–154. https://doi.org/10.1111/cge.14164
Chicago
Cui, Chong, Luping Zhang, Fuping Qian, Yuxin Chen, Bowei Huang, Fang Wang, Daqi Wang, et al. 2022. “A Humanized Murine Model, Demonstrating Dominant Progressive Hearing Loss Caused by a Novel KCNQ4 Mutation (p.G228D) from a Large Chinese Family.” Clinical Genetics 102 (2): 149–54. doi:10.1111/cge.14164.