==== Front Orphanet J Rare Dis Orphanet J Rare Dis Orphanet Journal of Rare Diseases 1750-1172 BioMed Central London 37386499 2791 10.1186/s13023-023-02791-6 Correction Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy Salman Mohd 12 Verma Anshuman 13 Chaurasia Sunita 4 Prasad Deeksha 12 Kannabiran Chitra 4 Singh Vivek viveksingh@lvpei.org 1 Ramappa Muralidhar muralidhar@lvpei.org 456 1 grid.417748.9 0000 0004 1767 1636 Prof. Brien Holden Eye Research Center, Champalimaud Translational Centre for Eye Research, L V Prasad Eye Institute, Hyderabad, India 2 grid.411639.8 0000 0001 0571 5193 Manipal Academy of Higher Education, Manipal, Karnataka India 3 MNR Foundation for Research and Innovations, MNR Medical College, MNR Nagar, Sangareddy, Telangana India 4 grid.417748.9 0000 0004 1767 1636 Centre for Rare Eye Diseases and Ocular Genetics, L V Prasad Eye Institute, Hyderabad, India 5 grid.417748.9 0000 0004 1767 1636 Jasti V Ramanamma Children’s Eye Care Center, L V Prasad Eye Institute, Hyderabad, India 6 grid.417748.9 0000 0004 1767 1636 The Cornea and Anterior Segment, L V Prasad Eye Institute, KAR Campus, Banjara Hills, Hyderabad, India 29 6 2023 29 6 2023 2023 18 170© The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/ Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. issue-copyright-statement© Institut National de la Santé et de la Recherche Médicale (INSERM) 2023 ==== Body pmcFollowing publication of the original article [1], we have been notified that the Ethics approval and consent to participate declarations should be as follows: The study was approved by the institutional review board of the L V Prasad Eye Institute (Ethics Ref. No. LEC-BHR-01–20–381). Written informed consent from all adult participants and legal guardians/parents for minors were obtained for the research study and publications.“Ethics approval and consent to participate” section on page no. 11 to be considered as stated above. However, the statement mentioned in the Ethics statement of Methods section on page no. 2 is correct. The online version of the original article can be found at 10.1186/s13023-022-02521-4. Publisher’s Note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Mohd Salman and Anshuman Verma contributed equally to this work. ==== Refs References 1. Salman et al. (2022) Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy (2022). 17:361 DOI: 10.1186/s13023-022-02521-4.