TTF2 Gene Mutation in Neonates with Congenital Hypothyroidism Caused by Thyroid Dysgenesis
Background: Thyroid transcription factor 2 (TTF2) or forkhead box E1 (FOXE1) is a polyalanine domain protein with an important role in the morphogenesis and development of thyroid gland. Mutations of TTF2 gene have been identified in neonates with congenital hypothyroidism caused by thyroid dysgenes...
| 出版年: | مجله دانشکده پزشکی اصفهان |
|---|---|
| 主要な著者: | , , , , |
| フォーマット: | 論文 |
| 言語: | ペルシア語 |
| 出版事項: |
Isfahan University of Medical Sciences
2012-07-01
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| オンライン･アクセス: | http://jims.mui.ac.ir/index.php/jims/article/view/1418 |