Bauer, Peter <br/><br/>
Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown cause.  [electronic resource] 

 -  Movement disorders : official journal of the Movement Disorder Society  Oct 2006 
 - 1734-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0885-3185 
<br/><br/><label>Standard No.: </label>10.1002/mds.21031  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Child<br/>Child, Preschool<br/>Chorea--diagnosis<br/>Chromosome Aberrations<br/>Female<br/>Finland<br/>Genes, Dominant<br/>Genotype<br/>Humans<br/>Infant<br/>Male<br/>Middle Aged<br/>Mutation--genetics<br/>Nuclear Proteins--genetics<br/>Polymerase Chain Reaction<br/>Thyroid Nuclear Factor 1<br/>Transcription Factors--genetics