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...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Persa |
| Έκδοση: |
Isfahan University of Medical Sciences
2012-07-01
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| Σειρά: | مجله دانشکده پزشکی اصفهان |
| Διαθέσιμο Online: | http://jims.mui.ac.ir/index.php/jims/article/view/1418 |
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