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OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium

Authors

  • Ajoy Vincent Department of Ophthalmology, The Hospital for Sick Children, Toronto, Ontario, Canada Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada University of Toronto, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Nicole Forster Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Jason T Maynes Department of Anesthesia and Pain Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada Program in Molecular Structure and Function, The Hospital for Sick Children, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Tara A Paton Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Gail Billingsley Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Nicole M Roslin Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Arfan Ali Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Joanne Sutherland Department of Ophthalmology, The Hospital for Sick Children, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Tom Wright Department of Ophthalmology, The Hospital for Sick Children, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Carol A Westall Department of Ophthalmology, The Hospital for Sick Children, Toronto, Ontario, Canada University of Toronto, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Andrew D Paterson Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada University of Toronto, Toronto, Ontario, Canada The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Christian R Marshall Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  • Google scholar articles
  • Elise Héon Department of Ophthalmology, The Hospital for Sick Children, Toronto, Ontario, Canada Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada University of Toronto, Toronto, Ontario, Canada PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Ajoy Vincent, Department of Ophthalmology and Vision Sciences, Hospital for Sick Children, 525 University Avenue, Suite 800, Toronto, Ontario, Canada M5G 1X8; ajoy.vincent{at}sickkids.ca, ajoyvincent{at}gmail.com
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Citation

Vincent A, Forster N, Maynes JT, et al
OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium

Publication history

  • Received July 4, 2014
  • Revised September 15, 2014
  • Accepted September 16, 2014
  • First published October 7, 2014.
Online issue publication 
November 17, 2014

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