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Add Bestrophin gene mutations cause canine multifocal retinopathy : a novel animal model for best disease

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Add Comparative genomic mapping of uncharacterized canine retinal ESTs to identify novel candidate genes for hereditary retinal disorders

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Add Independent origin and restricted distribution of RPGR deletions causing XLPRA

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Add Structural organization and expression pattern of the canine RPGRIP1 isoforms in retinal tissue

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Add Transcriptional profile analysis of RPGRORF15 frameshift mutation identifies novel genes associated with retinal degeneration

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