Li, J., Gao, B., Xiao, X., Li, S., Jia, X., Sun, W., . . . Zhang, Q. (2016). Exome sequencing identified null mutations in LOXL3 associated with early-onset high myopia. Mol Vis.
Citação norma ChicagoLi, Jiali, Bei Gao, Xueshan Xiao, Shiqiang Li, Xiaoyun Jia, Wenmin Sun, Xiangming Guo, and Qingjiong Zhang. "Exome Sequencing Identified Null Mutations in LOXL3 Associated With Early-onset High Myopia." Mol Vis 2016.
MLA citiranjeLi, Jiali, et al. "Exome Sequencing Identified Null Mutations in LOXL3 Associated With Early-onset High Myopia." Mol Vis 2016.
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