Shan, Din-E <br/><br/>
Presence of spinocerebellar ataxia type 2 gene mutation in a patient with apparently sporadic Parkinson's disease: clinical implications.  [electronic resource] 

 -  Movement disorders : official journal of the Movement Disorder Society  Nov 2004 
 - 1357-60 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/mds.20212  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Alleles<br/>Antiparkinson Agents--therapeutic use<br/>Ataxins<br/>Caudate Nucleus--diagnostic imaging<br/>DNA Mutational Analysis<br/>Dominance, Cerebral--physiology<br/>Genetic Carrier Screening<br/>Genetic Testing<br/>Humans<br/>Levodopa--therapeutic use<br/>Male<br/>Middle Aged<br/>Nerve Tissue Proteins<br/>Neurologic Examination<br/>Parkinson Disease--diagnostic imaging<br/>Polymerase Chain Reaction<br/>Positron-Emission Tomography<br/>Proteins--genetics<br/>Putamen--diagnostic imaging<br/>Spinocerebellar Ataxias--diagnostic imaging<br/>Treatment Outcome<br/>Trinucleotide Repeats<br/>Ubiquitin-Protein Ligases--genetics