Gibbs, Daniel <br/><br/>
Retinal pigment epithelium defects in humans and mice with mutations in MYO7A: imaging melanosome-specific autofluorescence.  [electronic resource] 

 -  Investigative ophthalmology & visual science  Sep 2009 
 - 4386-93 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-5783 
<br/><br/><label>Standard No.: </label>10.1167/iovs.09-3471  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Child<br/>Choroid--pathology<br/>Diagnostic Imaging--methods<br/>Disease Models, Animal<br/>Fluorescence<br/>Humans<br/>Melanosomes--pathology<br/>Mice<br/>Mice, Inbred C57BL<br/>Microscopy, Confocal<br/>Middle Aged<br/>Mutation<br/>Myosin VIIa<br/>Myosins--genetics<br/>Ophthalmoscopy<br/>Retinal Pigment Epithelium--pathology<br/>Tomography, Optical Coherence<br/>Usher Syndromes--diagnosis<br/>Young Adult