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EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa
Authors:Abd El-Aziz Mai M  Barragan Isabel  O'Driscoll Ciara A  Goodstadt Leo  Prigmore Elena  Borrego Salud  Mena Marcela  Pieras Juan I  El-Ashry Mohamed F  Safieh Leen Abu  Shah Amna  Cheetham Michael E  Carter Nigel P  Chakarova Christina  Ponting Chris P  Bhattacharya Shomi S  Antinolo Guillermo
Institution:Department of Molecular Genetics, Institute of Ophthalmology, London EC1V 9EL, UK.
Abstract:Using a positional cloning approach supported by comparative genomics, we have identified a previously unreported gene, EYS, at the RP25 locus on chromosome 6q12 commonly mutated in autosomal recessive retinitis pigmentosa. Spanning over 2 Mb, this is the largest eye-specific gene identified so far. EYS is independently disrupted in four other mammalian lineages, including that of rodents, but is well conserved from Drosophila to man and is likely to have a role in the modeling of retinal architecture.
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