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Stargardt disease: clinical features, molecular genetics, animal models and therapeutic options

Authors

  • Preena Tanna UCL Institute of Ophthalmology, University College London, London, UK Moorfields Eye Hospital, London, UK PubMed articlesGoogle scholar articles
  • Rupert W Strauss UCL Institute of Ophthalmology, University College London, London, UK Moorfields Eye Hospital, London, UK Departments of Ophthalmology, Medical University Graz and Johannes Kepler University, Linz, Austria PubMed articlesGoogle scholar articles
  • Kaoru Fujinami UCL Institute of Ophthalmology, University College London, London, UK Moorfields Eye Hospital, London, UK National Institute of Sensory Organs, National Hospital Organization, Tokyo Medical Centre, Tokyo, Japan PubMed articlesGoogle scholar articles
  • Michel Michaelides UCL Institute of Ophthalmology, University College London, London, UK Moorfields Eye Hospital, London, UK PubMed articlesGoogle scholar articles
  1. Correspondence to Michel Michaelides, UCL Institute of Ophthalmology, 11-43 Bath Street, London EC1V 9EL, UK; michel.michaelides{at}ucl.ac.uk
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Citation

Tanna P, Strauss RW, Fujinami K, et al
Stargardt disease: clinical features, molecular genetics, animal models and therapeutic options
British Journal of Ophthalmology 2017;101:25-30.

Publication history

  • Received April 4, 2016
  • Revised June 20, 2016
  • Accepted July 11, 2016
  • First published August 4, 2016.
Online issue publication 
December 14, 2016

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Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/