Angelini, C <br/><br/>
Homozygous alpha-sarcoglycan mutation in two siblings: one asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patient.  [electronic resource] 

 -  Muscle & nerve  Jun 1998 
 - 769-75 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0148-639X 
<br/><br/><label>Standard No.: </label>10.1002/(sici)1097-4598(199806)21:6<769::aid-mus9>3.0.co;2-5  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Anti-Inflammatory Agents--therapeutic use<br/>Biomarkers--analysis<br/>Biopsy<br/>Blotting, Western<br/>Creatine Kinase--metabolism<br/>Cytoskeletal Proteins--genetics<br/>Dystroglycans<br/>Female<br/>Humans<br/>Immunohistochemistry<br/>Male<br/>Membrane Glycoproteins--genetics<br/>Muscle, Skeletal--chemistry<br/>Muscular Dystrophies--diagnostic imaging<br/>Pedigree<br/>Polymerase Chain Reaction<br/>Pregnenediones--therapeutic use<br/>Sarcoglycans<br/>Tomography, X-Ray Computed<br/>Transcription, Genetic