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Acland, Gregory M

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Bestrophin gene mutations cause canine multifocal retinopathy : a novel animal model for best disease 17 15 0
Independent origin and restricted distribution of RPGR deletions causing XLPRA 9 9 0
Comparative genomic mapping of uncharacterized canine retinal ESTs to identify novel candidate genes for hereditary retinal disorders 17 17 0
Transcriptional profile analysis of RPGRORF15 frameshift mutation identifies novel genes associated with retinal degeneration 20 19 0
Structural organization and expression pattern of the canine RPGRIP1 isoforms in retinal tissue 10 10 0
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Acland, Gregory M

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Acland, Gregory M

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