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gene, article, retinitis, pigmentosa, protein, human, mouse, google, scholar, nature, dominant, cas, mutations, sequence, pim, autosomal, disease, residues, figure, retinal, shown, genet, analysis, data, keen, chromosome, identified, sequences, present, polymorphism, content, form, locus, family, mutation, genomic, patients, region, dna, genes, cir, conserved, exon, control, splicing, cookies, function, change, inglehearn, previously,

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nature portfolio permissions reprints privacy policy crispr/cas9-based mouse model retinal cdna libraries visual system development advertising open reading frame nature social media author information authors pre-mrna splicing factors author correspondence x-linked recessive modes emboss software suite permissions single-strand conformation polymorphism regional form putative mrna sequence �regional’ loss regional duplication mouse model bearing privacy retinitis pigmentosa european economic area transcriptional control complex journals search log specific physiological context explore content similar content full size image inverclyde royal hospital photoactivated molecular species inherited retinal degenerations multiple loci accounting erythrocyte pyrimidine 5-nucleotidase k210r polymorphism highlighted originally provoked interest high metabolic rate yac contig spanning cag repeat expansion bardet–biedl syndrome 9 accepting optional cookies developing avian retina disrupted alternative splicing inherited retinal dystrophies single rp patient expression profile based cgmp-binding domain washington genome center

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