Ma, Di <br/><br/>
A novel nonsense mutation in MYO15A is associated with non-syndromic hearing loss: a case report.  [electronic resource] 

 -  BMC medical genetics  08 2018 
 - 133 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1471-2350 
<br/><br/><label>Standard No.: </label>10.1186/s12881-018-0657-y  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Asian People--genetics<br/>Child<br/>Codon, Nonsense--genetics<br/>Deafness--genetics<br/>Female<br/>Genes, Recessive--genetics<br/>Hearing Loss--genetics<br/>Humans<br/>Male<br/>Myosins--genetics<br/>Pedigree