Human Genome Epidemiology Literature Finder
Records 1 - 1 (of 1 Records) |
Query Trace: Hypothyroidism and TAZ[original query] |
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Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesis. Journal of endocrinological investigation 2009 Mar 32 (3): 3. Ferrara AM, De Sanctis L, Rossi G, Capuano S, Del Prete G, Zampella E, Gianino P, Corrias A, Fenzi G, Zannini M, Macchia PE |
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- Page last updated:Apr 16, 2024
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