Investigation of the functional impact of CHED- and FECD4-associated SLC4A11 mutations in human corneal endothelial cells
Article in PLOS ONE (January 2024)
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Updates on congenital hereditary endothelial dystrophy
Article in Taiwan Journal of Ophthalmology (November 2023)
Correction to: identification and in silico analysis of a spectrum of SLC4A11 variations in indian familial and sporadic cases of congenital hereditary endothelial dystrophy
Article in Orphanet Journal of Rare Diseases (June 2023)