Identification of interacting protein partners of TOPORS in the retina

Retinitis pigmentosa (RP, MIM#268000) is a heterogeneous disease characterised by loss of rod photoreceptors and pigment deposits in the retina. Historically, genes linked to RP were associated with rod-specific functions. Recently, a novel class of ubiquitously expressed causative genes has emerged...

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Bibliographic Details
Main Author: Czub, B.
Other Authors: Bhattacharya, S. S.
Published: University College London (University of London) 2015
Subjects:
Online Access:https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.666806