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Clinical science
Original article
Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1
  1. Robert H Henderson1,2,3,
  2. Donna S Mackay2,
  3. Zheng Li2,
  4. Phillip Moradi1,2,3,
  5. Panagiotis Sergouniotis1,2,
  6. Isabelle Russell-Eggitt4,
  7. Dorothy A Thompson4,
  8. Anthony G Robson1,2,
  9. Graham E Holder1,2,
  10. Andrew R Webster1,2,
  11. Anthony T Moore1,2,3
  1. 1Moorfields Eye Hospital, London, UK
  2. 2UCL Institute of Ophthalmology, London, UK
  3. 3Great Ormond Street Hospital for Children, London, UK
  4. 4Ulverscroft Vision Research Group, Great Ormond Street Hospital for Children, London, UK
  1. Correspondence to Robert H Henderson, Professorial Unit, Moorfields Eye Hospital, 162 City Road, London EC1V 2PD, UK; r.henderson{at}ucl.ac.uk

https://doi.org/10.1136/bjo.2010.186882

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    Footnotes

    • Funding Fight for Sight, British Retinitis Pigmentosa Society, Ulverscroft foundation, Foundation Fighting Blindness USA, National Institute for Health Research (NIHR—Moorfields Biomedical Research Centre).

    • Competing interests None.

    • Patient consent Obtained.

    • Ethics approval Ethics approval was provided by the Moorfields Research Ethics Committee Approval Number (MOA1005).

    • Provenance and peer review Not commissioned; externally peer reviewed.