Brique, S <br/><br/>
A new GTP-cyclohydrolase I mutation in an unusual dopa-responsive dystonia, familial form.  [electronic resource] 

 -  Neuroreport  Feb 1999 
 - 487-91 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0959-4965 
<br/><br/><label>Standard No.: </label>10.1097/00001756-199902250-00008  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Amino Acid Sequence--genetics<br/>Base Sequence--genetics<br/>Child<br/>Dopamine--therapeutic use<br/>Dystonia--drug therapy<br/>Female<br/>GTP Cyclohydrolase--genetics<br/>Heterozygote<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation--physiology<br/>Pedigree