Grimes, D A <br/><br/>
Inherited myoclonus-dystonia: evidence supporting genetic heterogeneity.  [electronic resource] 

 -  Movement disorders : official journal of the Movement Disorder Society  Jan 2001 
 - 106-10 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0885-3185 
<br/><br/><label>Standard No.: </label>10.1002/1531-8257(200101)16:1<106::aid-mds1022>3.0.co;2-7  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>Child, Preschool<br/>Chromosomes, Human, Pair 11--genetics<br/>Dystonic Disorders--complications<br/>Female<br/>Genetic Linkage<br/>Humans<br/>Male<br/>Myoclonus--complications<br/>Pedigree<br/>Point Mutation--genetics<br/>Polymerase Chain Reaction<br/>Receptors, Dopamine D2--genetics