Wu, Y R <br/><br/>
Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease.  [electronic resource] 

 -  Clinical genetics  Mar 2004 
 - 209-14 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0009-9163 
<br/><br/><label>Standard No.: </label>10.1111/j.0009-9163.2004.00213.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Age of Onset<br/>Aged<br/>Case-Control Studies<br/>Female<br/>Gene Frequency<br/>Genetic Testing--methods<br/>Humans<br/>Middle Aged<br/>Myoclonic Epilepsies, Progressive--genetics<br/>Nerve Tissue Proteins--genetics<br/>Parkinson Disease--genetics<br/>Phenotype<br/>RNA, Long Noncoding<br/>RNA, Untranslated<br/>Spinocerebellar Ataxias--etiology<br/>TATA-Box Binding Protein--genetics<br/>Taiwan--epidemiology<br/>Trinucleotide Repeat Expansion