Guo, H., Li, J., Gao, F., Li, J., Wu, X., & Liu, Q. (2015). Whole-exome sequencing reveals a novel CHM gene mutation in a family with choroideremia initially diagnosed as retinitis pigmentosa. BMC Ophthalmol.

Guo, Hui, Jisheng Li, Fei Gao, Jiangxia Li, Xinyi Wu, و Qiji Liu. "Whole-exome Sequencing Reveals a Novel CHM Gene Mutation in a Family With Choroideremia Initially Diagnosed As Retinitis Pigmentosa." BMC Ophthalmol 2015.

Guo, Hui, et al. "Whole-exome Sequencing Reveals a Novel CHM Gene Mutation in a Family With Choroideremia Initially Diagnosed As Retinitis Pigmentosa." BMC Ophthalmol 2015.