1. Karahan, Mine, Demirtaş, Atılım Armağan, Erdem, Seyfettin, Tekeş, Selahattin, Keklikçi, Uğur. 2021. Crystalline gene mutations in Turkish children with congenital cataracts. In International ophthalmology, 41, 2847-2852. doi:10.1007/s10792-021-01843-9. https://pubmed.ncbi.nlm.nih.gov/33864186/
2. Ji, Yanan, Zhao, Xiangyu, Zhang, Juanmei, Zhao, Youcai, Zhao, Jun. 2020. A novel missense mutation of CRYBB1 causes congenital cataract in a Chinese family. In European journal of ophthalmology, 31, 1064-1069. doi:10.1177/1120672120914497. https://pubmed.ncbi.nlm.nih.gov/32223445/
3. Wang, Jun, Ma, Xu, Gu, Feng, Wang, Ning-li, Zhu, Si-quan. . A missense mutation S228P in the CRYBB1 gene causes autosomal dominant congenital cataract. In Chinese medical journal, 120, 820-4. doi:. https://pubmed.ncbi.nlm.nih.gov/17531125/
4. Limi, Saima, Zhao, Yilin, Guo, Peng, Skoultchi, Arthur I, Cvekl, Ales. . Bidirectional Analysis of Cryba4-Crybb1 Nascent Transcription and Nuclear Accumulation of Crybb3 mRNAs in Lens Fibers. In Investigative ophthalmology & visual science, 60, 234-244. doi:10.1167/iovs.18-25921. https://pubmed.ncbi.nlm.nih.gov/30646012/
5. Lenfant, Caroline, Baz, Patrick, Degavre, Anne, Zalloua, Pierre, Julier, Cécile. 2017. Juvenile-Onset Diabetes and Congenital Cataract: "Double-Gene" Mutations Mimicking a Syndromic Diabetes Presentation. In Genes, 8, . doi:10.3390/genes8110309. https://pubmed.ncbi.nlm.nih.gov/29112131/
6. Rao, Yan, Dong, Sufang, Li, Zuhua, Yan, Ming, Zheng, Fang. 2017. A novel truncation mutation in CRYBB1 associated with autosomal dominant congenital cataract with nystagmus. In Molecular vision, 23, 624-637. doi:. https://pubmed.ncbi.nlm.nih.gov/28928627/
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