1. Liu, Yuming, Ye, Zi, Yu, HanYang, Zhang, Yan, Li, Zhaohui. 2024. A novel base substitution mutation of the CRYBA2 gene is associated with autosomal dominant congenital cataract. In Gene, 927, 148726. doi:10.1016/j.gene.2024.148726. https://pubmed.ncbi.nlm.nih.gov/38909969/
2. Ma, Zhiwei, Chauss, Daniel, Disatham, Joshua, Kantorow, Marc, Hejtmancik, J Fielding. . Patterns of Crystallin Gene Expression in Differentiation State Specific Regions of the Embryonic Chicken Lens. In Investigative ophthalmology & visual science, 63, 8. doi:10.1167/iovs.63.4.8. https://pubmed.ncbi.nlm.nih.gov/35412582/
3. Kong, Yanbo, Yi, Haoan, Li, Fan, Zha, Xu, He, Yongshu. 2023. A novel missense mutation in the CRYBA2 caused autosomal dominant presenile cataract in a Chinese family. In Molecular genetics and genomics : MGG, 298, 1237-1244. doi:10.1007/s00438-023-02052-y. https://pubmed.ncbi.nlm.nih.gov/37438446/
4. Reis, Linda M, Tyler, Rebecca C, Muheisen, Sanaa, Power, Patricia, Semina, Elena V. 2013. Whole exome sequencing in dominant cataract identifies a new causative factor, CRYBA2, and a variety of novel alleles in known genes. In Human genetics, 132, 761-70. doi:10.1007/s00439-013-1289-0. https://pubmed.ncbi.nlm.nih.gov/23508780/
5. Xu, Jia-Sheng, Liao, Kai-Li, Wang, Xinlu, He, Jiarui, Wang, Xiao-Zhong. 2020. Combining bioinformatics techniques to explore the molecular mechanisms involved in pancreatic cancer metastasis and prognosis. In Journal of cellular and molecular medicine, 24, 14128-14138. doi:10.1111/jcmm.16023. https://pubmed.ncbi.nlm.nih.gov/33164330/