Damme, Markus <br/><br/>
Gene disruption of Mfsd8 in mice provides the first animal model for CLN7 disease.  [electronic resource] 

 -  Neurobiology of disease  May 2014 
 - 12-24 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1095-953X 
<br/><br/><label>Standard No.: </label>10.1016/j.nbd.2014.01.003  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Brain--metabolism<br/>Central Nervous System--metabolism<br/>Disease Models, Animal<br/>Gene Expression Regulation, Enzymologic--genetics<br/>Humans<br/>Kidney--enzymology<br/>Liver--enzymology<br/>Membrane Transport Proteins--genetics<br/>Mice<br/>Mice, Inbred C57BL<br/>Microscopy, Electron<br/>Neuronal Ceroid-Lipofuscinoses--genetics<br/>RNA, Messenger--genetics<br/>Retina--metabolism<br/>Subcellular Fractions--metabolism<br/>alpha-Mannosidase--metabolism<br/>beta-Galactosidase--metabolism<br/>beta-N-Acetylhexosaminidases--metabolism