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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...
Autores principales: | Kuot, Abraham, Hewitt, Alex W., Snibson, Grant R., Souzeau, Emmanuelle, Mills, Richard, Craig, Jamie E., Burdon, Kathryn P., Sharma, Shiwani |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5568371/ https://www.ncbi.nlm.nih.gov/pubmed/28832669 http://dx.doi.org/10.1371/journal.pone.0183719 |
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