APA

Li N., Xu Y., Li G., Yu T., Yao R., Wang X. & Wang J. (20170613). Exome sequencing identifies a de novo mutation of CTNNB1 gene in a patient mainly presented with retinal detachment, lens and vitreous opacities, microcephaly, and developmental delay: Case report and literature review. : Medicine.

Chicago

Li Niu, Xu Yufei, Li Guoqiang, Yu Tingting, Yao Ru-En, Wang Xiumin and Wang Jian. 20170613. Exome sequencing identifies a de novo mutation of CTNNB1 gene in a patient mainly presented with retinal detachment, lens and vitreous opacities, microcephaly, and developmental delay: Case report and literature review. : Medicine.

Harvard

Li N., Xu Y., Li G., Yu T., Yao R., Wang X. and Wang J. (20170613). Exome sequencing identifies a de novo mutation of CTNNB1 gene in a patient mainly presented with retinal detachment, lens and vitreous opacities, microcephaly, and developmental delay: Case report and literature review. : Medicine.

MLA

Li Niu, Xu Yufei, Li Guoqiang, Yu Tingting, Yao Ru-En, Wang Xiumin and Wang Jian. Exome sequencing identifies a de novo mutation of CTNNB1 gene in a patient mainly presented with retinal detachment, lens and vitreous opacities, microcephaly, and developmental delay: Case report and literature review. : Medicine. 20170613.