Duggan, D J <br/><br/>
alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutations.  [electronic resource] 

 -  Journal of the neurological sciences  Sep 1996 
 - 30-9 p.  digital 
<br/><br/> Publication Type: Case Reports; 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>0022-510X 
<br/><br/><label>Standard No.: </label>10.1016/0022-510x(96)00028-7  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Cytoskeletal Proteins--analysis<br/>Dystrophin--genetics<br/>Humans<br/>Immunoblotting<br/>Membrane Glycoproteins--analysis<br/>Molecular Sequence Data<br/>Muscular Dystrophies--genetics<br/>Mutation<br/>RNA, Messenger--metabolism<br/>Sarcoglycans