Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesis.

Academic Article
Publication Date:
2009
Iris type:
01.01 Articolo in rivista
List of contributors:
Authors of the University:
Handle:
https://iris.cnr.it/handle/20.500.14243/51230
Published in:
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION (TESTO STAMP.)
Journal