Associated Papers
Characterizing Retinal Sensitivity and Structure in Congenital Stationary Night Blindness: A Combined Microperimetry and OCT Study.
Yu M et al.
Investigative Ophthalmology & Visual Science, 2024
38916884 (PubMed )
Supplement: iovs-65-6-35_s002.xlsx › PMID-original
Mutation screening of the LRIT3, CABP4, and GPR179 genes in Chinese patients with Schubert-Bornschein congenital stationary night blindness.
Dan H et al.
Ophthalmic Genetics, 0
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