ロード中...
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...
保存先:
| 主要な著者: | , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
The Association for Research in Vision and Ophthalmology
2014
|
| 主題: | |
| オンライン･アクセス: | 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 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|