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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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Bibliografiset tiedot
Päätekijät: Mootha, V. Vinod, Gong, Xin, Ku, Hung-Chih, Xing, Chao
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: The Association for Research in Vision and Ophthalmology 2014
Aiheet:
Linkit: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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