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
Karin W. Littink 1, Patricia T.Y. Stappers 1, Frans C.C. Riemslag 1,2, Herman E. Talsma 1,2, Maria M. Van Genderen 2, Frans P.M. Cremers 3,4, Rob W.J. Collin 3,4
and L. Ingeborgh Van den Born 1,*
and L. Ingeborgh Van den Born 1,*
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)
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The authors wish to make the following correction to this paper [1]. [...] View Full-Text
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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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