Browsing by Subject "Distròfia corneal de Meesmann"
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A novel pathogenic variant in the KRT3 gene in a family with meesmann corneal dystrophy
(Journal of Clinical Medicine, 2025)Background/Objectives: to report a novel KRT3 Meesmann corneal dystrophy (MECD) mutation and its clinical findings in a Spanish family, thus completing the international database. Case series study. ...
