Cheillan, David <br/><br/>
Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms.  [electronic resource] 

 -  Orphanet journal of rare diseases  Dec 2012 
 - 96 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1750-1172 
<br/><br/><label>Standard No.: </label>10.1186/1750-1172-7-96  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Creatine--deficiency<br/>Creatinine--urine<br/>Female<br/>Glycine--analogs & derivatives<br/>Humans<br/>Male<br/>Nerve Tissue Proteins--genetics<br/>Nervous System Diseases--etiology<br/>Plasma Membrane Neurotransmitter Transport Proteins--genetics<br/>Retrospective Studies