GLRA2 gene mutations cause high myopia in humans and mice

Conclusion
GLRA2 was identified as a novel HM-causing gene. Its variants would cause HM through altered visual experience by impairing photoperception and visual transmission.

Source: Journal of Medical Genetics - January 24, 2023 Category: Genetics & Stem Cells Authors: Tian, Q., Tong, P., Chen, G., Deng, M., Cai, T., Tian, R., Zhang, Z., Xia, K., Hu, Z. Tags: Open access Novel disease loci Source Type: research