Gutiérrez Cortés, Nicolás <br/><br/>
Novel mitochondrial DNA mutations responsible for maternally inherited nonsyndromic hearing loss.  [electronic resource] 

 -  Human mutation  Apr 2012 
 - 681-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.22023  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aminoglycosides--adverse effects<br/>Cell Line<br/>Cell Respiration--genetics<br/>Cytochromes b--genetics<br/>DNA, Mitochondrial<br/>Female<br/>Hearing Loss--chemically induced<br/>Humans<br/>Male<br/>Mitochondria--genetics<br/>Mothers<br/>Mutation<br/>NADH Dehydrogenase--chemistry<br/>Pedigree<br/>Phosphorylation<br/>Polymorphism, Restriction Fragment Length<br/>Protein Conformation<br/>RNA, Transfer, Ile--genetics<br/>RNA, Transfer, Ser--genetics