Selleri, S <br/><br/>
Deletion of exons 11-17 and novel mutations of the galactocerebrosidase gene in adult- and early-onset patients with Krabbe disease.  [electronic resource] 

 -  Journal of neurology  Nov 2000 
 - 875-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0340-5354 
<br/><br/><label>Standard No.: </label>10.1007/s004150070076  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Brain--pathology<br/>Exons<br/>Female<br/>Galactosylceramidase--genetics<br/>Gene Deletion<br/>Humans<br/>Leukodystrophy, Globoid Cell--genetics<br/>Magnetic Resonance Imaging<br/>Male<br/>Mutation--genetics<br/>Time Factors