For citations:
Ivanova M.E., Gorgisheli K.V., Zolnikova I.V., Atarshchikov D.S., Barh D., Salmasi Zh.M., Balashova L.M. Pathogenesis and clinical features of congenital stationary night blindness in case of c.283delC NYX gene mutation. Russian Ophthalmological Journal. 2019;12(3):77-84. (In Russ.) https://doi.org/10.21516/2072-0076-2019-12-3-77-84