1. Khan, Sarmir, Rana, Nehal, Nasir, Hilal, Khan, Luqman, Khan, Muhammad. 2023. Mutational analysis of CRYAA gene of cataract and investigating risk assessment factors responsible for eye diseases in district buner, KPK, Pakistan. In Cellular and molecular biology (Noisy-le-Grand, France), 69, 1-7. doi:10.14715/cmb/2023.69.9.1. https://pubmed.ncbi.nlm.nih.gov/37807341/
2. Song, Zixun, Si, Nuo, Xiao, Wei. 2018. A novel mutation in the CRYAA gene associated with congenital cataract and microphthalmia in a Chinese family. In BMC medical genetics, 19, 190. doi:10.1186/s12881-018-0695-5. https://pubmed.ncbi.nlm.nih.gov/30340470/
3. Yu, Hongtao, Liu, Kaifeng, Lu, Peirong. 2021. Polymorphisms in CRYAA Promoter with Susceptibility to Cataract: A Meta-Analysis. In Seminars in ophthalmology, 36, 429-436. doi:10.1080/08820538.2021.1903943. https://pubmed.ncbi.nlm.nih.gov/34010109/
4. Zhang, Lu, Zhang, Yi, Liu, Ping, Tang, Xianling, Su, Sheng. 2011. Congenital anterior polar cataract associated with a missense mutation in the human alpha crystallin gene CRYAA. In Molecular vision, 17, 2693-7. doi:. https://pubmed.ncbi.nlm.nih.gov/22065922/
5. Beby, Francis, Commeaux, Claire, Bozon, Muriel, Edery, Patrick, Morlé, Laurette. . New phenotype associated with an Arg116Cys mutation in the CRYAA gene: nuclear cataract, iris coloboma, and microphthalmia. In Archives of ophthalmology (Chicago, Ill. : 1960), 125, 213-6. doi:. https://pubmed.ncbi.nlm.nih.gov/17296897/
6. 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/