Pegoraro, E <br/><br/>
A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophy.  [electronic resource] 

 -  Neurology  Oct 2000 
 - 1128-34 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>0028-3878 
<br/><br/><label>Standard No.: </label>10.1212/wnl.55.8.1128  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Alternative Splicing<br/>Exons<br/>Female<br/>Humans<br/>Laminin--analysis<br/>Magnetic Resonance Imaging<br/>Muscles--chemistry<br/>Muscular Dystrophies--congenital<br/>Mutation--genetics<br/>Phenotype<br/>Protein Isoforms--genetics