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Clinical science
Autosomal recessive retinitis pigmentosa with RP1 mutations is associated with myopia

Authors

  • Thomas Chassine Maladies Sensorielles Génétiques, CHRU, Montpellier, France PubMed articlesGoogle scholar articles
  • Béatrice Bocquet INSERM U1051, Institute for Neurosciences of Montpellier, Montpellier, France Université Montpellier 1, Montpellier, France Université Montpellier 2, Montpellier, France PubMed articlesGoogle scholar articles
  • Vincent Daien Université Montpellier 1, Montpellier, France INSERM U1061, Montpellier, France Department of Ophthalmology, CHRU, Montpellier, France PubMed articlesGoogle scholar articles
  • Almudena Avila-Fernandez Department of Genetics, Instituto de Investigación Sanitaria-Fundación Jimenez Diaz, University Hospital, Madrid, Spain Centre for Biomedical Network Research on Rare Diseases (CIBERER), ISCIII, Madrid, Spain PubMed articlesGoogle scholar articles
  • Carmen Ayuso Department of Genetics, Instituto de Investigación Sanitaria-Fundación Jimenez Diaz, University Hospital, Madrid, Spain Centre for Biomedical Network Research on Rare Diseases (CIBERER), ISCIII, Madrid, Spain PubMed articlesGoogle scholar articles
  • Rob WJ Collin Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, The Netherlands PubMed articlesGoogle scholar articles
  • Marta Corton Department of Genetics, Instituto de Investigación Sanitaria-Fundación Jimenez Diaz, University Hospital, Madrid, Spain Centre for Biomedical Network Research on Rare Diseases (CIBERER), ISCIII, Madrid, Spain PubMed articlesGoogle scholar articles
  • J Fielding Hejtmancik Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, Bethesda, Maryland, USA PubMed articlesGoogle scholar articles
  • L Ingeborgh van den Born The Rotterdam Eye Hospital, Rotterdam, The Netherlands PubMed articlesGoogle scholar articles
  • B Jeroen Klevering Department of Ophthalmology, Radboud University Medical Center, Nijmegen, The Netherlands PubMed articlesGoogle scholar articles
  • S Amer Riazuddin National Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan The Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA PubMed articlesGoogle scholar articles
  • Nathacha Sendon Maladies Sensorielles Génétiques, CHRU, Montpellier, France PubMed articlesGoogle scholar articles
  • Annie Lacroux INSERM U1051, Institute for Neurosciences of Montpellier, Montpellier, France Université Montpellier 1, Montpellier, France Université Montpellier 2, Montpellier, France PubMed articlesGoogle scholar articles
  • Isabelle Meunier Maladies Sensorielles Génétiques, CHRU, Montpellier, France INSERM U1051, Institute for Neurosciences of Montpellier, Montpellier, France Université Montpellier 1, Montpellier, France Université Montpellier 2, Montpellier, France PubMed articlesGoogle scholar articles
  • Christian P Hamel Maladies Sensorielles Génétiques, CHRU, Montpellier, France INSERM U1051, Institute for Neurosciences of Montpellier, Montpellier, France Université Montpellier 1, Montpellier, France Université Montpellier 2, Montpellier, France PubMed articlesGoogle scholar articles
  1. Correspondence to Professor Christian P Hamel, INSERM U1051, Institut des Neurosciences de Montpellier, Hôpital Saint-Eloi, BP 74103, 80, rue Augustin Fliche, 34091 Montpellier Cedex 5, France; christian.hamel{at}inserm.fr
  2. TC and BB contributed equally
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Citation

Chassine T, Bocquet B, Daien V, et al
Autosomal recessive retinitis pigmentosa with RP1 mutations is associated with myopia
British Journal of Ophthalmology 2015;99:1360-1365.

Publication history

  • Received October 4, 2014
  • Revised March 13, 2015
  • Accepted March 26, 2015
  • First published April 16, 2015.
Online issue publication 
August 23, 2023

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