Rohacek, Alex M <br/><br/>
ESRP1 Mutations Cause Hearing Loss due to Defects in Alternative Splicing that Disrupt Cochlear Development.  [electronic resource] 

 -  Developmental cell  11 2017 
 - 318-331.e5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1878-1551 
<br/><br/><label>Standard No.: </label>10.1016/j.devcel.2017.09.026  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alternative Splicing--genetics<br/>Animals<br/>Cell Differentiation--genetics<br/>Cochlea--embryology<br/>Hearing Loss--genetics<br/>Mice, Knockout<br/>Mutation--genetics<br/>RNA-Binding Proteins--genetics