Identification of NovelRPGRORF15 Mutations in X-linked Progressive Cone-Rod Dystrophy (XLCORD) Families

Author:

Ebenezer Neil D.1,Michaelides Michel2,Jenkins Sharon A.3,Audo Isabelle3,Webster Andrew R.2,Cheetham Michael E.4,Stockman Andrew5,Maher Eamonn R.6,Ainsworth John R.7,Yates John R.8,Bradshaw Keith9,Holder Graham E.4,Moore Anthony T.2,Hardcastle Alison J.1

Affiliation:

1. From the Divisions of Molecular Genetics,

2. From the Divisions of Molecular Genetics,3Moorfields Eye Hospital, London, United Kingdom; the

3. Moorfields Eye Hospital, London, United Kingdom; the

4. Pathology, and

5. Visual Science, Institute of Ophthalmology, University College London, United Kingdom;

6. Section of Medical and Molecular Genetics, Department of Paediatrics and Child Health, University of Birmingham, The Medical School, Birmingham, United Kingdom;

7. Birmingham Midlands Eye Hospital and Birmingham Children’s Hospital, Birmingham, United Kingdom; the

8. Department of Medical Genetics, University of Cambridge, Cambridge, United Kingdom; and the

9. Department of Ophthalmology, Addenbrookes Hospital, Cambridge, United Kingdom.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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