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Congenital Stationary Night Blindness: Structure, Function and Genotype-Phenotype Correlations in a Cohort of 122 Patients.
Katta Mohamed, de Guimaraes Thales A C, Fujinami-Yokokawa Yu, Fujinami Kaoru, Georgiou Michalis, Mahroo Omar A et al.
Ophthalmol RetinaMar 202410 citationsCase Series
This study of 122 CSNB patients found stable retinal structure and visual acuity over time, with specific genetic variants (NYX, TRPM1) linked to myopia, aiding prognosis.