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Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy
Orphanet Journal of Rare Diseases volume 18, Article number: 170 (2023)
The Original Article was published on 17 September 2022
Following 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.
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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: https://doi.org/10.1186/s13023-022-02521-4.
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Salman, M., Verma, A., Chaurasia, S. et al. Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy. Orphanet J Rare Dis 18, 170 (2023). https://doi.org/10.1186/s13023-023-02791-6
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DOI: https://doi.org/10.1186/s13023-023-02791-6