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Association and Familial Segregation of CTG18.1 Trinucleotide Repeat Expansion of TCF4 Gene in Fuchs' Endothelial Corneal Dystrophy
PURPOSE. We tested the association between two intronic polymorphisms (CTG18.1 and rs613872) in TCF4 and Fuchs' endothelial corneal dystrophy (FECD), and analyzed their segregation patterns in families. METHODS. We recruited 120 unrelated Caucasian subjects with FECD and 100 controls. Available...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Association for Research in Vision and Ophthalmology
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3880006/ https://ncbi.nlm.nih.gov/pubmed/24255041 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.13-12611 |
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