Dong, Mingrui <br/><br/>
DAG1 mutations associated with asymptomatic hyperCKemia and hypoglycosylation of α-dystroglycan.  [electronic resource] 

 -  Neurology  Jan 2015 
 - 273-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/WNL.0000000000001162  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Cell Line, Transformed<br/>Cohort Studies<br/>Creatine Kinase--metabolism<br/>Dystroglycans--genetics<br/>Dystrophin--metabolism<br/>Female<br/>Genetic Association Studies<br/>Glycosylation<br/>Humans<br/>Laminin--metabolism<br/>Male<br/>Metabolic Diseases--complications<br/>Middle Aged<br/>Muscle, Skeletal--pathology<br/>Muscular Dystrophies--complications<br/>Mutation--genetics<br/>Phenotype<br/>Protein Transport--genetics<br/>Transfection