Identification of a novel protein interacting with RPGR
X-linked retinitis pigmentosa is a severe form of human retinal degeneration and is most commonly caused by mutations in the <i>RPGR</i> gene, which maps to chromosomal region Xp21.1. The <i>RPGR</i> gene product is a novel protein containing an amino terminal domain that is...
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University of Edinburgh
2001
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| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.641859 |