Orphanet Journal of Rare Diseases (Jun 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

  • Mohd Salman,
  • Anshuman Verma,
  • Sunita Chaurasia,
  • Deeksha Prasad,
  • Chitra Kannabiran,
  • Vivek Singh,
  • Muralidhar Ramappa

DOI
https://doi.org/10.1186/s13023-023-02791-6
Journal volume & issue
Vol. 18, no. 1
pp. 1 – 1

Abstract

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