Funder
National Institute for Health Research Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology
Reference83 articles.
1. Identification of a photoreceptor cell-specific nuclear receptor;Kobayashi;Proc Natl Acad Sci U S A,1999
2. NR2E3 mutations in enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), and retinitis pigmentosa (RP);Schorderet;Hum Mutat,2009
3. Recurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosa;Coppieters;Am J Hum Gen,2007
4. The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish Inquisition;Gerber;Hum Genet,2000
5. Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and clumped pigmentary retinal degeneration;Sharon;Invest Ophthalmol Vis Sci,2002
Cited by
33 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献