Ferrara, A M <br/><br/>
Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesis.  [electronic resource] 

 -  Journal of endocrinological investigation  Mar 2009 
 - 238-41 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1720-8386 
<br/><br/><label>Standard No.: </label>10.1007/BF03346459  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acyltransferases<br/>Case-Control Studies<br/>DNA Mutational Analysis<br/>Gene Frequency<br/>Genetic Testing<br/>Humans<br/>Mutation--physiology<br/>Nuclear Proteins--metabolism<br/>PAX8 Transcription Factor<br/>Paired Box Transcription Factors--metabolism<br/>Polymorphism, Single-Stranded Conformational<br/>Thyroid Dysgenesis--genetics<br/>Thyroid Nuclear Factor 1<br/>Trans-Activators--genetics<br/>Transcription Factors--genetics