Lattanzi, G <br/><br/>
Unusual laminin alpha2 processing in myoblasts from a patient with a novel variant of congenital muscular dystrophy.  [electronic resource] 

 -  Biochemical and biophysical research communications  Nov 2000 
 - 639-42 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0006-291X 
<br/><br/><label>Standard No.: </label>10.1006/bbrc.2000.3735  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cell Differentiation<br/>Child, Preschool<br/>Female<br/>Humans<br/>Laminin--metabolism<br/>Matrix Metalloproteinase 2--metabolism<br/>Matrix Metalloproteinases--metabolism<br/>Matrix Metalloproteinases, Membrane-Associated<br/>Metalloendopeptidases--metabolism<br/>Muscular Dystrophies--enzymology