Ormazabal, Aida <br/><br/>
Deletion in the tyrosine hydroxylase gene in a patient with a mild phenotype.  [electronic resource] 

 -  Movement disorders : official journal of the Movement Disorder Society  Jul 2011 
 - 1558-60 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1531-8257 
<br/><br/><label>Standard No.: </label>10.1002/mds.23564  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Antiparkinson Agents--therapeutic use<br/>Carbidopa--therapeutic use<br/>DNA Mutational Analysis<br/>Drug Combinations<br/>Female<br/>Homovanillic Acid--cerebrospinal fluid<br/>Humans<br/>Infant<br/>Levodopa--therapeutic use<br/>Movement Disorders--cerebrospinal fluid<br/>Phenotype<br/>Sequence Deletion--genetics<br/>Tyrosine 3-Monooxygenase--genetics<br/>Video Recording