학술논문
Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesis
Document Type
Article
Author
Source
In: Journal of Endocrinological Investigation . (Journal of Endocrinological Investigation, March 2009, 32(3):238-241)
Subject
Language
English
ISSN
03914097