Gene expression in the corneal endothelium of Fuchs endothelial corneal dystrophy patients with and without expansion of a trinucleotide repeat in TCF4

Fuchs Endothelial Corneal Dystrophy (FECD) is a late onset, autosomal dominant eye disease that can lead to loss of vision. Expansion of a CTG trinucleotide repeat in the third intron of the transcription factor 4 (TCF4) gene is highly associated with FECD. However, only about 75% of FECD patients i...

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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Wieben, Eric D., Aleff, Ross A., Tang, Xiaojia, Kalari, Krishna R., Maguire, Leo J., Patel, Sanjay V., Baratz, Keith H., Fautsch, Michael P.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2018
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6028112/
https://ncbi.nlm.nih.gov/pubmed/29966009
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0200005
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