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. 2020 May 3;11(5):503. doi: 10.3390/genes11050503

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

Imen Habibi 1,*, Yosra Falfoul 2, Margarita G Todorova 3,4, Stefan Wyrsch 5, Veronika Vaclavik 6, Maria Helfenstein 5, Ahmed Turki 2, Khaled El Matri 2, Leila El Matri 2, Daniel F Schorderet 1,7,8
PMCID: PMC7288654  PMID: 32375275

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. doi: 10.3390/genes10120953. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 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 doi: 10.1111/ceo.13577. [DOI] [PubMed] [Google Scholar]

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