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

✍ Scribed by Ferrara, A. M.; Sanctis, L.; Rossi, G.; Capuano, S.; Prete, G.; Zampella, E.; Gianino, P.; Corrias, A.; Fenzi, G.; Zannini, M.; Macchia, P. E.

Book ID: 125336728
Publisher: Springer-Verlag
Year: 2009
Tongue: English
Weight: 171 KB
Volume: 32
Category: Article
ISSN: 0391-4097
DOI: 10.1007/BF03346459

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