A novel COL4A5 splicing mutation causes alport syndrome in a Chinese family.

MLA

Chen, Suyun, et al. “A Novel COL4A5 Splicing Mutation Causes Alport Syndrome in a Chinese Family.” BMC Medical Genomics, vol. 17, no. 1, Apr. 2024, pp. 1–9. EBSCOhost, https://doi.org/10.1186/s12920-024-01878-8.

APA

Chen, S., Xu, G., Zhao, Z., Du, J., Shen, B., & Li, C. (2024). A novel COL4A5 splicing mutation causes alport syndrome in a Chinese family. BMC Medical Genomics, 17(1), 1–9. https://doi.org/10.1186/s12920-024-01878-8

Chicago

Chen, Suyun, Guangbiao Xu, Zhixin Zhao, Juping Du, Bo Shen, and Chunping Li. 2024. “A Novel COL4A5 Splicing Mutation Causes Alport Syndrome in a Chinese Family.” BMC Medical Genomics 17 (1): 1–9. doi:10.1186/s12920-024-01878-8.