Association of NR2E3 but Not NRL Mutations with Retinitis Pigmentosa in the Chinese Population
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AbstractPURPOSE. Mutations in the NR2E3 and NRL genes have been implicated in both autosomal dominant and autosomal recessive retinitis pigmentosa (RP). In this study, the mutation profiles of these two genes were investigated in Chinese RP patients.
All Author(s) ListYang YP, Zhang X, Chen LJ, Chiang SWY, Tam POS, Lai TYY, Chan CKM, Wang NL, Lam DSC, Pang CP
Journal nameInvestigative Ophthalmology & Visual Science
Volume Number51
Issue Number4
PublisherAssociation for Research in Vision and Ophthalmology (ARVO)
Pages2229 - 2235
LanguagesEnglish-United Kingdom
Web of Science Subject CategoriesOphthalmology; OPHTHALMOLOGY

Last updated on 2021-25-02 at 23:54