Giannantonio, Sara <br/><br/>
Genetic identification and molecular modeling characterization of a novel POU3F4 variant in two Italian deaf brothers.  [electronic resource] 

 -  International journal of pediatric otorhinolaryngology  Feb 2020 
 - 109790 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1872-8464 
<br/><br/><label>Standard No.: </label>10.1016/j.ijporl.2019.109790  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child, Preschool<br/>Deafness--genetics<br/>Female<br/>Genetic Diseases, X-Linked--genetics<br/>Hearing Loss, Conductive--genetics<br/>Hearing Loss, Sensorineural--genetics<br/>Humans<br/>Infant<br/>Italy<br/>Male<br/>Models, Molecular<br/>Mutation, Missense<br/>POU Domain Factors--chemistry<br/>Pedigree<br/>Protein Folding<br/>Siblings