McMahon, Anne <br/><br/>
A Stargardt disease-3 mutation in the mouse Elovl4 gene causes retinal deficiency of C32-C36 acyl phosphatidylcholines.  [electronic resource] 

 -  FEBS letters  Nov 2007 
 - 5459-63 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0014-5793 
<br/><br/><label>Standard No.: </label>10.1016/j.febslet.2007.10.050  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Cell Extracts<br/>Eye Proteins--genetics<br/>Heterozygote<br/>Mass Spectrometry<br/>Membrane Proteins--genetics<br/>Mice<br/>Mice, Transgenic<br/>Mutation--genetics<br/>Phosphatidylcholines--chemistry<br/>Protein Folding<br/>RNA, Messenger--genetics<br/>Retina--metabolism