Miteff, F <br/><br/>
Clinical and laboratory features of patients with myophosphorylase deficiency (McArdle disease).  [electronic resource] 

 -  Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia  Aug 2011 
 - 1055-8 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1532-2653 
<br/><br/><label>Standard No.: </label>10.1016/j.jocn.2010.12.033  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Amino Acids--genetics<br/>Creatine Kinase--blood<br/>DNA Mutational Analysis<br/>Female<br/>Glycogen Phosphorylase--genetics<br/>Glycogen Phosphorylase, Muscle Form--deficiency<br/>Glycogen Storage Disease Type V--diagnosis<br/>Humans<br/>Male<br/>Middle Aged<br/>Muscle, Skeletal--pathology<br/>Mutation--genetics<br/>Retrospective Studies<br/>Young Adult