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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
Open AccessEditorial

Special Issue Introduction: Inherited Retinal Disease: Novel Candidate Genes, Genotype–Phenotype Correlations, and Inheritance Models

1
Department of Human Genetics and Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands
2
Department of Ophthalmology, Leiden University Medical Center, P.O. Box 9600, 2300 RC Leiden, The Netherlands
3
Academic Medical Center, Department of Ophthalmology, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands
4
Ocular Genomics Institute, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, MA 02114, USA
5
Sorbonne Université, INSERM, CNRS, Institut de la Vision, Department of Genetics, 17 rue Moreau, 75012 Paris, France
*
Authors to whom correspondence should be addressed.
Genes 2018, 9(4), 215; https://doi.org/10.3390/genes9040215
Received: 5 April 2018 / Accepted: 13 April 2018 / Published: 16 April 2018
Note: In lieu of an abstract, this is an excerpt from the first page.

Inherited retinal diseases (IRDs) are genetically and clinically heterogeneous disorders.[...] View Full-Text
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Cremers, F.P.M.; Boon, C.J.F.; Bujakowska, K.; Zeitz, C. Special Issue Introduction: Inherited Retinal Disease: Novel Candidate Genes, Genotype–Phenotype Correlations, and Inheritance Models. Genes 2018, 9, 215.

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