Article info
Genotype-phenotype correlations
Original article
Compound heterozygosity for severe and hypomorphic NDUFS2 mutations cause non-syndromic LHON-like optic neuropathy
- Correspondence to Doctor Jean-Michel Rozet, Laboratory of Genetics in Ophthalmology (LGO), Institute of genetic diseases, Imagine, 24 boulevard du Montparnasse, Paris 75015, France; jean-michel.rozet{at}inserm.fr
- Professor Ulrich Brandt, Radboud Center for Mitochondrial Medicine (RCMM), Radboud University Medical Centre, Geert Grooteplein-Zuid 10, Route 772, 6525 GA Nijmegen, The Netherlands; Ulrich.brandt{at}radboudumc.nl
Citation
Compound heterozygosity for severe and hypomorphic NDUFS2 mutations cause non-syndromic LHON-like optic neuropathy
Publication history
- Received August 4, 2016
- Revised November 29, 2016
- Accepted December 1, 2016
- First published December 28, 2016.
Online issue publication
April 24, 2017
Article Versions
- Previous version (28 December 2016).
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