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Minimal is famous about whether clients with complete congenital stationary night blindness (CSN keep artistic function in their lifetime. The goal of this report was to describe clinical and genetic attributes of an elderly feminine patient with full CSNB that people observed for 5years. Molecular genetic analysis making use of whole-exome sequencing (WES) ended up being done to detect disease-causing variations. We performed a thorough ophthalmic examination including full-field electroretinography (E
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