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Correction

Correction: Habibi I. et al. “Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)” Genes, 2019, 10, 953

1
IRO-Institute for Research in Ophthalmology, 1950 Sion, Switzerland
2
Oculogenetic laboratory LR14SP01, Hedi Rais Institute of Ophthalmology (Department B), Tunis 1007, Tunisia
3
Department of Ophthalmology, Cantonal Hospital St. Gallen, 9000 St. Gallen, Switzerland
4
Department of Ophthalmology, University of Basel, 4000 Basel, Switzerland
5
Eye Clinic, Lucerne Cantonal Hospital, 6000 Lucerne, Switzerland
6
Jules Gonin Eye Hospital, 1004 Lausanne, Switzerland
7
Department of Ophthalmology, University of Lausanne, 1004 Lausanne, Switzerland
8
Faculty of Life Sciences, Ecole polytechnique fédérale de Lausanne, 1004 Lausanne, Switzerland
*
Author to whom correspondence should be addressed.
Genes 2020, 11(5), 503; https://doi.org/10.3390/genes11050503
Submission received: 9 April 2020 / Revised: 26 April 2020 / Accepted: 30 April 2020 / Published: 3 May 2020
(This article belongs to the Special Issue Recent Advances in Inherited Eye Disease)
The authors wish to make a correction to the published version of their paper [1] because they misread a finding that they cited from the article by Chibani et al. [2] (This reference is cited as [9] in the original text.).
In the second paragraph of Section 4.2, the sentence “This alteration was not reported in the 1000 Genome Project or in the ExAC database and was only recently reported in compound heterozygous state [9].” should be changed to “This alteration was not reported in the 1000 Genome Project or in the ExAC database but has recently been found [9].”
The authors would like to apologize for any inconvenience caused. The change does not affect the scientific results. The manuscript will be updated and the original will remain online on the article webpage, with a reference to this correction.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Habibi, I.; Falfoul, Y.; Todorova, M.G.; Wyrsch, S.; Vaclavik, V.; Helfenstein, M.; Turki, A.; Matri, K.E.; Matri, L.E.; Schorderet, D.F. Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB). Genes 2019, 10, 953. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Chibani, Z.; Abid, I.Z.; Molbaek, A.; Söderkvist, P.; Feki, J.; Hmani-Aifa, M. Novel BEST1 gene mutations associated with two different forms of macular dystrophy in Tunisian families. Clin. Exp. Ophthalmol. 2019. [Google Scholar] [CrossRef] [PubMed]

Share and Cite

MDPI and ACS Style

Habibi, I.; Falfoul, Y.; Todorova, M.G.; Wyrsch, S.; Vaclavik, V.; Helfenstein, M.; Turki, A.; El Matri, K.; El Matri, L.; Schorderet, D.F. Correction: Habibi I. et al. “Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)” Genes, 2019, 10, 953. Genes 2020, 11, 503. https://doi.org/10.3390/genes11050503

AMA Style

Habibi I, Falfoul Y, Todorova MG, Wyrsch S, Vaclavik V, Helfenstein M, Turki A, El Matri K, El Matri L, Schorderet DF. Correction: Habibi I. et al. “Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)” Genes, 2019, 10, 953. Genes. 2020; 11(5):503. https://doi.org/10.3390/genes11050503

Chicago/Turabian Style

Habibi, Imen, Yosra Falfoul, Margarita G. Todorova, Stefan Wyrsch, Veronika Vaclavik, Maria Helfenstein, Ahmed Turki, Khaled El Matri, Leila El Matri, and Daniel F. Schorderet. 2020. "Correction: Habibi I. et al. “Clinical and Genetic Findings of Autosomal Recessive Bestrophinopathy (ARB)” Genes, 2019, 10, 953" Genes 11, no. 5: 503. https://doi.org/10.3390/genes11050503

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