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Visualitzant per matèria "Tomografia de coherència òptica del segment anterior"

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    • A novel pathogenic variant in the KRT3 gene in a family with meesmann corneal dystrophy 

      De Faria, Alix; Charoenrook, Víctor; Larena, Raquel; Ferragut Alegre, Álvaro; Valero, Rebeca; Julio, Gemma; Barraquer, Rafael I (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. ...