McNally, E M <br/><br/>
Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy.  [electronic resource] 

 -  Human molecular genetics  Nov 1996 
 - 1841-7 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>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/5.11.1841  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Child<br/>Cytoskeletal Proteins<br/>Dystrophin--analysis<br/>Frameshift Mutation--genetics<br/>Genes, Recessive--genetics<br/>Homozygote<br/>Humans<br/>In Vitro Techniques<br/>Italy<br/>Male<br/>Membrane Glycoproteins--analysis<br/>Molecular Sequence Data<br/>Muscle, Skeletal--chemistry<br/>Muscular Dystrophies--genetics<br/>Mutation--genetics<br/>Polymorphism, Single-Stranded Conformational<br/>Sarcoglycans<br/>Sequence Deletion--genetics<br/>Sequence Homology, Amino Acid<br/>United States