Journal of Ophthalmology
Volume 2018 (2018), Article ID 3039672, 1 page
https://doi.org/10.1155/2018/3039672

Corrigendum

Corrigendum to “Mutation Spectrum of the ABCA4 Gene in a Greek Cohort with Stargardt Disease: Identification of Novel Mutations and Evidence of Three Prevalent Mutated Alleles”

Smaragda Kamakari,¹ Vassiliki Kokkinou,¹ George Koutsodontis,¹ Polixeni Stamatiou,¹ Christoforos Giatzakis,² Anastasios Anastasakis,³ Ioannis Minas Aslanides,⁴ Stavrenia Koukoula,⁵ Theoni Panagiotoglou,⁶ Ioannis Datseris,⁷ and Miltiadis K. Tsilimbaris⁶

¹Ophthalmic Genetics Unit, OMMA Ophthalmological Institute of Athens, Athens, Greece
²DNAbiolab, Cretan Center for Research and Development of Applications on Genetics and Molecular Biology, Heraklion, Crete, Greece
³Department of Clinical Electrophysiology of Vision, Athens Eye Hospital, Glyfada, Athens, Greece
⁴Department of Ophthalmology, Emmetropia Mediterranean Eye Institute, Heraklion, Crete, Greece
⁵Ophthalmica Institute of Ophthalmology and Microsurgery, Thessaloniki, Greece
⁶Department of Ophthalmology, University of Crete School of Medicine, Heraklion, Greece
⁷Department of Retinal Disorders, OMMA Ophthalmological Institute of Athens, Athens, Greece

Correspondence should be addressed to Smaragda Kamakari; kamakari@hotmail.gr

Received 19 August 2018; Accepted 1 November 2018; Published 16 December 2018

Copyright © 2018 Smaragda Kamakari et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

In the article titled “Mutation Spectrum of the ABCA4 Gene in a Greek Cohort with Stargardt Disease: Identification of Novel Mutations and Evidence of Three Prevalent Mutated Alleles” [1], the first and last names of all the authors were reversed. The revised authors’ list is shown above.

References

K. Smaragda, K. Vassiliki, K. George et al., “Mutation spectrum of the ABCA4 gene in a Greek cohort with Stargardt disease: identification of novel mutations and evidence of three prevalent mutated alleles,” Journal of Ophthalmology, vol. 2018, Article ID 5706142, 10 pages, 2018.