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Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions

Authors

  1. Correspondence to Professor Michel Michaelides, UCL Institute of Ophthalmology, 11-43 Bath Street, London, EC1V 9EL, UK; Michel.Michaelides{at}moorfields.nhs.uk
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Citation

Kumaran N, Moore AT, Weleber RG, et al
Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions

Publication history

  • Received 23 November 2016
  • Revised 26 April 2017
  • Accepted 30 April 2017
  • Published online 8 July 2017.

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