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In the published article, there was an error in the legend for Figure 4 as published. The gene names corresponding to color degradation for the Waardenburg syndrome pie chart are incorrect.
Figure 4. Genetic spectrum of syndromic deafness in the Tunisian population. Deafness syndromes with known molecular etiologies are represented by pie charts. Each syndromic deafness is indicated with a different color. Color degradation has been adopted to specify the gene(s) associated with each syndrome. The number of patients carrying variants in each gene is provided.
The corrected legend appears below: The SOX10 gene should be at the top (darkest blue), and the EDNRB gene should be at the bottom (lightest blue). Consequently, the number of patients should be 8 for the SOX10 gene and 2 for the EDNRB gene.
In addition, there was an error in the caption of Figure 4 in the published version of the manuscript: “FIGURE 4: Genetic and mutational spectrum of syndromic deafness in the Tunisian population. Deafness syndromes with known molecular etiologies are represented by pie charts. Each syndromic deafness is indicated with a different color. Color degradation has been adopted to specify the gene(s) associated with each syndrome. The number of variants identified in each gene is provided.”
The corrected Figure 4 appears below:
The authors apologize for these errors and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Keywords: syndromic deafness (SD), spectrum of SDs, next-generation sequencing (NGS), early detection, under-diagnosis, Tunisia
Citation: Mkaouar R, Riahi Z, Marrakchi J, Mezzi N, Romdhane L, Boujemaa M, Dallali H, Sayeb M, Lahbib S, Jaouadi H, Boudabbous H, Zekri L, Chargui M, Messaoud O, Elyounsi M, Kraoua I, Zaouak A, Turki I, Mokni M, Boucher S, Petit C, Giraudet F, Mbarek C, Besbes G, Halayem S, Zainine R, Turki H, Tounsi A, Bonnet C, Mrad R, Abdelhak S, Trabelsi M and Charfeddine C (2024) Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health. Front. Genet. 15:1437233. doi: 10.3389/fgene.2024.1437233
Received: 23 May 2024; Accepted: 27 May 2024;
Published: 25 June 2024.
Edited and reviewed by:
Ferran Casals, University of Barcelona, SpainCopyright © 2024 Mkaouar, Riahi, Marrakchi, Mezzi, Romdhane, Boujemaa, Dallali, Sayeb, Lahbib, Jaouadi, Boudabbous, Zekri, Chargui, Messaoud, Elyounsi, Kraoua, Zaouak, Turki, Mokni, Boucher, Petit, Giraudet, Mbarek, Besbes, Halayem, Zainine, Turki, Tounsi, Bonnet, Mrad, Abdelhak, Trabelsi and Charfeddine. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Rahma Mkaouar, rahma.mkaouar@fst.utm.tn
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