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Clinical characterisation of a family with retinal dystrophy caused by mutation in the Mertk gene
  1. M Tschernutter1,
  2. S A Jenkins4,
  3. N H Waseem2,
  4. Z Saihan3,
  5. G E Holder4,
  6. A C Bird4,
  7. S S Bhattacharya2,
  8. R R Ali1,
  9. A R Webster3
  1. 1Division of Molecular Therapy, Institute of Ophthalmology, University College, London EC1V 9EL, UK
  2. 2Division of Molecular Genetics, Institute of Ophthalmology, University College, London EC1V 9EL, UK
  3. 3Division of Inherited Eye Disease, Institute of Ophthalmology, University College, London EC1V 9EL, UK
  4. 4Moorfields Eye Hospital, London EC1V 2PD, UK
  1. Correspondence to: Dr Andrew R Webster Institute of Ophthalmology, Bath Street, London EC1V 9EL, UK; andrew.webster{at}ucl.ac.uk

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