Gospe, S M <br/><br/>
Asymptomatic McArdle's disease associated with hyper-creatine kinase-emia and absence of myophosphorylase.  [electronic resource] 

 -  Neurology  Oct 1998 
 - 1228-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0028-3878 
<br/><br/><label>Standard No.: </label>10.1212/wnl.51.4.1228  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Creatine Kinase--blood<br/>Female<br/>Glycogen Storage Disease Type V--genetics<br/>Humans<br/>Muscle, Skeletal--enzymology<br/>Mutation<br/>Phosphorylases--blood<br/>Polymorphism, Restriction Fragment Length