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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