Long, X., Huang, Y., Tan, H., Li, Z., Zhang, R., Linpeng, S., . . . Wu, L. (2018). Identification of a novel MIP frameshift mutation associated with congenital cataract in a Chinese family by whole-exome sequencing and functional analysis. Eye (Lond).
Chicago Stili AlıntıLong, Xigui, et al. "Identification of a Novel MIP Frameshift Mutation Associated With Congenital Cataract in a Chinese Family By Whole-exome Sequencing and Functional Analysis." Eye (Lond) 2018.
MLA AlıntıLong, Xigui, et al. "Identification of a Novel MIP Frameshift Mutation Associated With Congenital Cataract in a Chinese Family By Whole-exome Sequencing and Functional Analysis." Eye (Lond) 2018.
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