Libby, R T <br/><br/>
Electroretinographic anomalies in mice with mutations in Myo7a, the gene involved in human Usher syndrome type 1B.  [electronic resource] 

 -  Investigative ophthalmology & visual science  Mar 2001 
 - 770-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0146-0404 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aging<br/>Animals<br/>Dark Adaptation<br/>Deafness--genetics<br/>Dyneins<br/>Electroretinography<br/>Female<br/>Male<br/>Mice<br/>Mice, Inbred BALB C<br/>Mice, Inbred C3H<br/>Mice, Inbred C57BL<br/>Mice, Inbred CBA<br/>Mice, Mutant Strains<br/>Mutation<br/>Myosin VIIa<br/>Myosins--genetics<br/>Retina--physiopathology<br/>Retinal Degeneration--genetics<br/>Syndrome