TCF4-mediated Fuchs endothelial corneal dystrophy: Insights into a common trinucleotide repeat-associated disease

Fuchs endothelial corneal dystrophy (FECD) is a common cause for heritable visual loss in the elderly. Since the first description of an association between FECD and common polymorphisms situated within the transcription factor 4 (TCF4) gene, genetic and molecular studies have implicated an intronic...

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Dettagli Bibliografici
Pubblicato in:Prog Retin Eye Res
Autori principali: Fautsch, Michael P., Wieben, Eric D., Baratz, Keith H., Bhattacharyya, Nihar, Sadan, Amanda N., Hafford-Tear, Nathaniel J., Tuft, Stephen J., Davidson, Alice E.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Pergamon 2021
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7988464/
https://ncbi.nlm.nih.gov/pubmed/32735996
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.preteyeres.2020.100883
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