Pupo, Altair Cadrobbi <br/><br/>
Study of a Brazilian family presenting non-syndromic hearing loss with mitochondrial inheritance.  [electronic resource] 

 -  Brazilian journal of otorhinolaryngology   
 - 786-789 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1808-8694 
<br/><br/><label>Standard No.: </label>10.1016/S1808-8694(15)31392-6  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Audiometry<br/>Brazil<br/>Child<br/>Child, Preschool<br/>DNA, Mitochondrial--genetics<br/>Genes, Mitochondrial--genetics<br/>Genetic Predisposition to Disease<br/>Hearing Loss--genetics<br/>Hearing Loss, Sensorineural--genetics<br/>Humans<br/>Middle Aged<br/>Mutation<br/>Pedigree