van den Heuvel, L P <br/><br/>
A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population.  [electronic resource] 

 -  Human genetics  Jun 1998 
 - 644-6 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/s004390050756  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosomes, Human, Pair 11<br/>Denmark<br/>Dystonia--drug therapy<br/>Genes, Recessive<br/>Humans<br/>Levodopa--therapeutic use<br/>Point Mutation<br/>Polymorphism, Single-Stranded Conformational<br/>Tyrosine 3-Monooxygenase--genetics