del Castillo, F J <br/><br/>
Maternally inherited non-syndromic hearing impairment in a Spanish family with the 7510T>C mutation in the mitochondrial tRNA(Ser(UCN)) gene.  [electronic resource] 

 -  Journal of medical genetics  Dec 2002 
 - e82 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.39.12.e82  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>DNA, Mitochondrial--genetics<br/>Female<br/>Hearing Loss--genetics<br/>Heterozygote<br/>Humans<br/>Male<br/>Pedigree<br/>Phenotype<br/>Point Mutation--genetics<br/>RNA, Transfer, Ser--genetics<br/>Spain