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Inherited causes of combined vision and hearing loss: clinical features and molecular genetics

Authors

  • Thales Antonio Cabral de Guimaraes Moorfields Eye Hospital NHS Foundation Trust, London, UK UCL Institute of Ophthalmology, University College London, London, UK PubMed articlesGoogle scholar articles
  • Elizabeth Arram Moorfields Eye Hospital NHS Foundation Trust, London, UK UCL Institute of Ophthalmology, University College London, London, UK PubMed articlesGoogle scholar articles
  • Ahmed F Shakarchi Jones Eye Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA PubMed articlesGoogle scholar articles
  • Michalis Georgiou Moorfields Eye Hospital NHS Foundation Trust, London, UK UCL Institute of Ophthalmology, University College London, London, UK Jones Eye Institute, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA PubMed articlesGoogle scholar articles
  • Michel Michaelides Moorfields Eye Hospital NHS Foundation Trust, London, UK UCL Institute of Ophthalmology, University College London, London, UK PubMed articlesGoogle scholar articles
  1. Correspondence to Michel Michaelides, Moorfields Eye Hospital NHS Foundation Trust, London, UK; michel.michaelides{at}ucl.ac.uk
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Citation

Guimaraes TACD, Arram E, Shakarchi AF, et al
Inherited causes of combined vision and hearing loss: clinical features and molecular genetics
British Journal of Ophthalmology 2023;107:1403-1414.

Publication history

  • Received May 9, 2022
  • Accepted September 7, 2022
  • First published September 26, 2022.
Online issue publication 
October 18, 2023

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© Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.