Functional characterisation of TOPORS, implicated in autosomal dominant retinitis pigmentosa
Purpose: Retinitis pigmentosa is a form of inherited retinal degeneration, whereby the rod photoreceptors are gradually lost. Patients usually manifest symptoms in the third decade of life, beginning with night blindness and loss of peripheral vision gradually progressing to tunnel vision and eventu...
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University College London (University of London)
2009
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| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.625170 |