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Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome
Correction to Genes 2018, 9(2), 68.
Correction

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
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.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. I. 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

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