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

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

doi:10.3390/genes9030145

Open AccessCorrection

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

by

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,*

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

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

with

The authors would like to apologize for any inconvenience caused to the readers by these changes.

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/).

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MDPI and ACS Style

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. 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. https://doi.org/10.3390/genes9030145

AMA Style

Littink KW, Stappers PTY, Riemslag FCC, Talsma HE, Van Genderen MM, Cremers FPM, Collin RWJ, Van den Born LI. Correction: Littink, K. W.; et al. Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes 2018, 9, 68. Genes. 2018; 9(3):145. https://doi.org/10.3390/genes9030145

Chicago/Turabian Style

Littink, Karin W., Patricia T.Y. Stappers, Frans C.C. Riemslag, Herman E. Talsma, Maria M. Van Genderen, Frans P.M. Cremers, Rob W.J. Collin, and L. Ingeborgh Van den Born. 2018. "Correction: Littink, K. W.; et al. Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes 2018, 9, 68" Genes 9, no. 3: 145. https://doi.org/10.3390/genes9030145

APA Style

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. (2018). Correction: Littink, K. W.; et al. Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes 2018, 9, 68. Genes, 9(3), 145. https://doi.org/10.3390/genes9030145

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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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