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
Differential stability of variant OPN1LW gene transcripts in myopic patients.
Mountford JK et al.
Molecular Vision, 2019
De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone Monochromacy.
Buena-Atienza E et al.
Scientific Reports, 2016
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