Associated Papers
The causal mutation in ARR3 gene for high myopia and progressive color vision defect.
Gu L et al.
Scientific Reports, 2023
Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction.
Stingl K et al.
International Journal of Molecular Sciences, 2022
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