Identification and characterisation of RP2 interacting proteins
Retinitis pigmentosa (RP) is a genetically and clinically heterogenous retinal degenerative disease, which is characterised by night blindness and constriction of visual fields in the early stages which progress to blindness. X-linked RP (XLRP) is the most severe form of the disease and 2 causative...
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University College London (University of London)
2007
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Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.498707 |