Citterio, Cintia E <br/><br/>
Novel mutational mechanism in the thyroglobulin gene: imperfect DNA inversion as a cause for hereditary hypothyroidism.  [electronic resource] 

 -  Molecular and cellular endocrinology  Dec 2013 
 - 220-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1872-8057 
<br/><br/><label>Standard No.: </label>10.1016/j.mce.2013.07.034  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Congenital Hypothyroidism--genetics<br/>Consanguinity<br/>DNA Mutational Analysis<br/>Genetic Association Studies<br/>Humans<br/>Introns<br/>Male<br/>Molecular Sequence Data<br/>Pedigree<br/>Polymorphism, Single Nucleotide<br/>Sequence Deletion<br/>Sequence Inversion<br/>Thyroglobulin--deficiency