TGC repeat expansion in the TCF4 gene increases the risk of Fuchs’ endothelial corneal dystrophy in Australian cases

Fuchs’ endothelial corneal dystrophy (FECD) is a progressive, vision impairing disease. Common single nucleotide polymorphisms (SNPs) and a trinucleotide repeat polymorphism, thymine-guanine-cytosine (TGC), in the TCF4 gene have been associated with the risk of FECD in some populations. We previousl...

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Detalles Bibliográficos
Publicado en:PLoS One
Main Authors: Kuot, Abraham, Hewitt, Alex W., Snibson, Grant R., Souzeau, Emmanuelle, Mills, Richard, Craig, Jamie E., Burdon, Kathryn P., Sharma, Shiwani
Formato: Artigo
Idioma:Inglês
Publicado: Public Library of Science 2017
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Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5568371/
https://ncbi.nlm.nih.gov/pubmed/28832669
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0183719
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