Zhang, L., Li, H., Zeng, J., Yang, Y., & Ding, C. (2018). Knobloch syndrome caused by homozygous frameshift mutation of the COL18A1 gene in a Chinese pedigree. International journal of ophthalmology, 11(6), 918-922. https://doi.org/10.18240/ijo.2018.06.04
Chicago Style (17th ed.) CitationZhang, Lu-Si, Hai-Bo Li, Jun Zeng, Yan Yang, and Chun Ding. "Knobloch Syndrome Caused by Homozygous Frameshift Mutation of the COL18A1 Gene in a Chinese Pedigree." International Journal of Ophthalmology 11, no. 6 (2018): 918-922. https://doi.org/10.18240/ijo.2018.06.04.
MLA (9th ed.) CitationZhang, Lu-Si, et al. "Knobloch Syndrome Caused by Homozygous Frameshift Mutation of the COL18A1 Gene in a Chinese Pedigree." International Journal of Ophthalmology, vol. 11, no. 6, 2018, pp. 918-922, https://doi.org/10.18240/ijo.2018.06.04.