Fujita, N <br/><br/>
Targeted disruption of the mouse sphingolipid activator protein gene: a complex phenotype, including severe leukodystrophy and wide-spread storage of multiple sphingolipids.  [electronic resource] 

 -  Human molecular genetics  Jun 1996 
 - 711-25 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/5.6.711  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Gene Deletion<br/>Glycoproteins--genetics<br/>Leukodystrophy, Metachromatic--etiology<br/>Mice<br/>Mice, Knockout<br/>Phenotype<br/>Protein Precursors--genetics<br/>Saposins<br/>Sphingolipid Activator Proteins<br/>Sphingolipids--metabolism