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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 November 23, 2016
  • Revised April 26, 2017
  • Accepted April 30, 2017
  • First published July 8, 2017.

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