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Ophthopedia Update:“Congenital Stationary Night Blindness: Structure, Function and Genotype – Phenotype Correlations in a cohort of 122 patients.”: To examine the molecular causes of Schubert-Bornschein (S-B) congenital stationary night blindness (CSNB), clinically characterize in detail, and assess genotype-phenotype correlations for retinal function and structure. #Ophthalmology #Retina #Ophthotwitter

“Congenital Stationary Night Blindness: Structure, Function and Genotype – Phenotype Correlations in a cohort of 122 patients.”

“Congenital Stationary Night Blindness: Structure, Function and Genotype – Phenotype Correlations in a cohort of 122 patients.”

ophthalmologyretina.org

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