Sewry, C A <br/><br/>
Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain.  [electronic resource] 

 -  Neuromuscular disorders : NMD  May 1997 
 - 169-75 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0960-8966 
<br/><br/><label>Standard No.: </label>10.1016/s0960-8966(97)00425-2  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Antibody Specificity<br/>Biopsy<br/>Child<br/>Child, Preschool<br/>Female<br/>Genetic Linkage<br/>Humans<br/>Immunohistochemistry<br/>Laminin--deficiency<br/>Male<br/>Muscle, Skeletal--chemistry<br/>Muscular Dystrophies--congenital<br/>Phenotype