Identiｦcations and in silico analysis of a spectrum of SLC4A11 mutations in Indian familial and non- familial cases of congenital hereditary endothelial dystrophy Mohd Salman LV Prasad Eye Institute Anshuman Verma (  vermaamrf@gmail.com ) MNR Medical College and Hospital https://orcid.org/0000-0003-0948-0154 Sunita Chaurasia LV Prasad Eye Institute Deeksha Prasad LV Prasad Eye Institute Chitra Kannabiran LV Prasad Eye Institute Vivek Singh LV Prasad Eye Institute MURALIDHAR RAMAPPA LV Prasad Eye Institute https://orcid.org/0000-0003-3667-5483 Research Article Keywords: CHED, SLC4A11, Corneal dystrophy, Mutations Posted Date: May 13th, 2022 DOI: https://doi.org/10.21203/rs.3.rs-1623088/v1 License:   This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License