The authors wish it to be known that, in their opinion, the first two authors should be regarded as joint First Authors.
RP1L1 Variants are Associated with a Spectrum of Inherited Retinal Diseases Including Retinitis Pigmentosa and Occult Macular Dystrophy
Article first published online: 17 JAN 2013
© 2012 Wiley Periodicals, Inc.
Volume 34, Issue 3, pages 506–514, March 2013
How to Cite
Davidson, A. E., Sergouniotis, P. I., Mackay, D. S., Wright, G. A., Waseem, N. H., Michaelides, M., Holder, G. E., Robson, A. G., Moore, A. T., Plagnol, V. and Webster, A. R. (2013), RP1L1 Variants are Associated with a Spectrum of Inherited Retinal Diseases Including Retinitis Pigmentosa and Occult Macular Dystrophy. Hum. Mutat., 34: 506–514. doi: 10.1002/humu.22264
Communicated by Daniel F. Schorderet
Contract grant sponsors: RP Fighting Blindness (formerly British Retinitis Pigmentosa Society); Moorfields Eye Hospital Special Trustees; Fight for Sight (Mercer Fund); National Institute for Health Research UK (Moorfields Eye Hospital and Institute of Ophthalmology Biomedical Research Centre, London, UK); the Foundation Fighting Blindness (USA); UK Medical Research Council (G1001158); Macular Disease Society UK.
- Issue published online: 18 FEB 2013
- Article first published online: 17 JAN 2013
- Accepted manuscript online: 21 DEC 2012 06:05AM EST
- Manuscript Accepted: 5 DEC 2012
- Manuscript Received: 21 SEP 2012
- RP Fighting Blindness (formerly British Retinitis Pigmentosa Society)
- Moorfields Eye Hospital Special Trustees
- Fight for Sight (Mercer Fund)
- National Institute for Health Research UK (Moorfields Eye Hospital and Institute of Ophthalmology Biomedical Research Centre, London, UK)
- the Foundation Fighting Blindness (USA)
- UK Medical Research Council. Grant Number: G1001158
- Macular Disease Society UK
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