Hypomorphic CDHR1 variants may result in retinitis pigmentosa with relative preservation of cone function

Soma Faraga Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK;b Nuffield Laboratory of Ophthalmology, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UKCorrespondence[email protected]

https://orcid.org/0000-0003-1758-6653 View further author information

Imran H. Yusufa Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK;b Nuffield Laboratory of Ophthalmology, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UKView further author information

Maria Kaukonena Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UKView further author information

Laura J. Taylora Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK;b Nuffield Laboratory of Ophthalmology, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UKView further author information

Peter Charbel Issaa Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK;b Nuffield Laboratory of Ophthalmology, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UKView further author information

Robert E. MacLarena Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK;b Nuffield Laboratory of Ophthalmology, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UKView further author information

Hypomorphic CDHR1 variants may result in retinitis pigmentosa with relative preservation of cone function

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Hypomorphic CDHR1 variants may result in retinitis pigmentosa with relative preservation of cone function

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