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Paper Details

Sub-cellular level resolution of common genetic variation in the photoreceptor layer identifies continuum between rare disease and common variation.
PLoS Genet
4
2023
111 loci, PRC, PRCs, PRPH2, Photoreceptor cells, VSX2, genes, genetic variants, light-detecting cells, ocular diseases, photoreceptor layer, rare disease, rare eye, retinal dystrophies, retinitis pigmentosa
Author NameAffiliation
Praveen J PatelNIHR Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology
Andrew R WebsterNIHR Biomedical Research Centre, Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology
Ewan BirneyEuropean Bioinformatics Institute
Ewan BirneyEuropean Bioinformatics Institute
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