Correction of
Genes 2018, 9(2), 68.
Correction: Littink, K. W.; et al. Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes 2018, 9, 68
1
The Rotterdam Eye Hospital, 3011 BH Rotterdam, The Netherlands
2
Bartiméus Center for Complex Visual Disorders, 3703 AJ Zeist, The Netherlands
3
Department of Human Genetics, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands
4
Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands
*
Author to whom correspondence should be addressed.
Genes 2018, 9(3), 145; https://doi.org/10.3390/genes9030145
Received: 2 March 2018 / Revised: 5 March 2018 / Accepted: 5 March 2018 / Published: 7 March 2018
(This article belongs to the Special Issue Inherited Retinal Disease: Novel Candidate Genes, Genotype–Phenotype Correlations and Inheritance Models)
Note: In lieu of an abstract, this is an excerpt from the first page.
The authors wish to make the following correction to this paper [1]. [...] View Full-Text
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MDPI and ACS Style
Littink, K.W.; Stappers, P.T.; Riemslag, F.C.; Talsma, H.E.; Van Genderen, M.M.; Cremers, F.P.; Collin, R.W.; Van den Born, L.I. Correction: Littink, K. W.; et al. Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes 2018, 9, 68. Genes 2018, 9, 145.
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