Correction: Littink, K. W.; et al. Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes 2018, 9, 68

Karin W. Littink; Patricia T.Y. Stappers; Frans C.C. Riemslag; Herman E. Talsma; Maria M. Van Genderen; Frans P.M. Cremers; Rob W.J. Collin; L. Ingeborgh Van den Born

doi:10.3390/genes9030145

,

and

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

Genes2018, 9(3), 145;https://doi.org/10.3390/genes9030145

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 []. Due to mislabeling, replace: Genes 09 00145 g001

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Reference

Littink, K.W.; Stappers, P.T.Y.; Riemslag, F.C.C.; Talsma, H.E.; van Genderen, M.M.; Cremers, F.P.M.; Collin, R.W.J.; van den Born, L.I. Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes 2018, 9, 68. [Google Scholar] [CrossRef] [PubMed]

© 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

Correction: Littink, K. W.; et al. Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes 2018, 9, 68

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