Duggan, D J <br/><br/>
Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2).  [electronic resource] 

 -  Neurogenetics  May 1997 
 - 49-58 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1364-6745 
<br/><br/><label>Standard No.: </label>10.1007/s100480050008  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosomes, Human, Pair 5<br/>Cytoskeletal Proteins--chemistry<br/>DNA Mutational Analysis<br/>Dystrophin--genetics<br/>Fluorescent Antibody Technique<br/>Follow-Up Studies<br/>Genes, Recessive<br/>Humans<br/>Membrane Glycoproteins--chemistry<br/>Microsatellite Repeats<br/>Muscle, Skeletal--metabolism<br/>Muscular Dystrophies--genetics<br/>Mutation<br/>Phenotype<br/>Polymorphism, Single-Stranded Conformational<br/>Protein Structure, Secondary<br/>Reverse Transcriptase Polymerase Chain Reaction<br/>Sarcoglycans