TCF4 trinucleotide repeat expansion in Swedish cases with Fuchs' endothelial corneal dystrophy

Abstract Purpose Fuchs' endothelial corneal dystrophy (FECD) has been considered a genetically heterogeneous disease but is increasingly associated with the transcription factor 4 ( TCF4 ) gene. This study investigates the prevalence of the cytosine‐thymine‐guanine (CTG) n repeat expansion in T...

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Bibliographic Details
Published in:Acta Ophthalmologica
Main Authors: Viberg, Andreas, Westin, Ida Maria, Golovleva, Irina, Byström, Berit
Other Authors: Stiftelsen Kronprinsessan Margaretas Arbetsnämnd för Synskadade, Ögonfonden
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2021
Subjects:
Online Access:http://dx.doi.org/10.1111/aos.15032
https://onlinelibrary.wiley.com/doi/pdf/10.1111/aos.15032
https://onlinelibrary.wiley.com/doi/full-xml/10.1111/aos.15032