Scaglia, Paula A <br/><br/>
Severe congenital non-autoimmune hyperthyroidism associated to a mutation in the extracellular domain of thyrotropin receptor gene.  [electronic resource] 

 -  Arquivos brasileiros de endocrinologia e metabologia  Nov 2012 
 - 513-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1677-9487 
<br/><br/><label>Standard No.: </label>10.1590/s0004-27302012000800009  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Female<br/>Humans<br/>Hyperthyroidism--congenital<br/>Infant, Newborn<br/>Mutation<br/>Pedigree<br/>Receptors, Thyrotropin--genetics<br/>Severity of Illness Index<br/>Thyroidectomy