ThePROM1Mutation p.R373C Causes an Autosomal Dominant Bull's Eye Maculopathy Associated with Rod, Rod–Cone, and Macular Dystrophy

Author:

Michaelides Michel1,Gaillard Marie-Claire2,Escher Pascal3,Tiab Leila3,Bedell Matthew4,Borruat François-Xavier2,Barthelmes Daniel5,Carmona Ruben4,Zhang Kang4,White Edward6,McClements Michelle7,Robson Anthony G.1,Holder Graham E.1,Bradshaw Keith8,Hunt David M.7,Webster Andrew R.1,Moore Anthony T.1,Schorderet Daniel F.9,Munier Francis L.10

Affiliation:

1. From the UCL Institute of Ophthalmology, London, United Kingdom; 2Moorfields Eye Hospital, London, United Kingdom;

2. Hôpital Ophtalmique Jules Gonin, Lausanne, Switzerland;

3. Institut de Recherche en Ophtalmologie, Sion, Switzerland;

4. the Department of Ophthalmology, Shiley Eye Center, University of California San Diego, San Diego, California;

5. the Department of Ophthalmology, University Hospital Zurich, Zurich, Switzerland;

6. Moorfields Eye Hospital, London, United Kingdom;

7. From the UCL Institute of Ophthalmology, London, United Kingdom;

8. the Department of Ophthalmology, Addenbrooke's Hospital, Cambridge, United Kingdom; and

9. Institut de Recherche en Ophtalmologie, Sion, Switzerland; 9EPFL (Ecole Polytechnique Fédérale de Lausanne), Lausanne, Switzerland.

10. Hôpital Ophtalmique Jules Gonin, Lausanne, Switzerland; 5Institut de Recherche en Ophtalmologie, Sion, Switzerland;

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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