Homo sapiens opsin 1, medium wave sensitive (OPN1MW), RefSeqGene on ch - Nucleotide

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The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy. [Proc Natl Acad Sci U S A. 2022]
The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy.
Wissinger B, Baumann B, Buena-Atienza E, Ravesh Z, Cideciyan AV, Stingl K, Audo I, Meunier I, Bocquet B, Traboulsi EI, et al. Proc Natl Acad Sci U S A. 2022 Jul 5; 119(27):e2115538119. Epub 2022 Jun 27.
Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction. [Int J Mol Sci. 2022]
Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction.
Stingl K, Baumann B, De Angeli P, Vincent A, Héon E, Cordonnier M, De Baere E, Raskin S, Sato MT, Shiokawa N, et al. Int J Mol Sci. 2022 Jun 20; 23(12). Epub 2022 Jun 20.
Intermixing the OPN1LW and OPN1MW Genes Disrupts the Exonic Splicing Code Causing an Array of Vision Disorders. [Genes (Basel). 2021]
Intermixing the OPN1LW and OPN1MW Genes Disrupts the Exonic Splicing Code Causing an Array of Vision Disorders.
Neitz M, Neitz J. Genes (Basel). 2021 Jul 29; 12(8). Epub 2021 Jul 29.

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Homo sapiens opsin 1, medium wave sensitive (OPN1MW), RefSeqGene on chromosome X
Homo sapiens opsin 1, medium wave sensitive (OPN1MW), RefSeqGene on chromosome X
gi|2296125290|ref|NG_011606.2|

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