Comprehensive Assessment of Genetic Variants Within TCF4 in Fuchs' Endothelial Corneal Dystrophy

PURPOSE. The single nucleotide variant (SNV), rs613872, in the transcription factor 4 (TCF4) gene was previously found to be strongly associated (P = 6 × 10(−26)) with Fuchs' endothelial corneal dystrophy (FECD). Subsequently, an intronic expansion of the repeating trinucleotides, TGC, was foun...

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Κύριοι συγγραφείς: Wieben, Eric D., Aleff, Ross A., Eckloff, Bruce W., Atkinson, Elizabeth J., Baheti, Saurabh, Middha, Sumit, Brown, William L., Patel, Sanjay V., Kocher, Jean-Pierre A., Baratz, Keith H.
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: The Association for Research in Vision and Ophthalmology 2014
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Articles
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4179444/
https://ncbi.nlm.nih.gov/pubmed/25168903
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.14-14958
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