A novel missense mutation in the NYX gene associated with high myopia

ConclusionsOne novel missense NYX mutation was identified in an adult male presented with high myopia, but without the major electrophysiological features normally associated with CSNB1A. NYX gene mutations may be considered as one of the rare genetic risk factors for high myopia without key features of CSNB1A. (Source: Ophthalmic and Physiological Optics)