Nirenberg, Melissa J <br/><br/>
Multiple system atrophy in a patient with the spinocerebellar ataxia 3 gene mutation.  [electronic resource] 

 -  Movement disorders : official journal of the Movement Disorder Society  Jan 2007 
 - 251-4 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0885-3185 
<br/><br/><label>Standard No.: </label>10.1002/mds.21231  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Ataxin-3<br/>Autopsy<br/>Cerebellum--metabolism<br/>DNA Repeat Expansion--genetics<br/>Fatal Outcome<br/>Female<br/>Humans<br/>Inclusion Bodies--metabolism<br/>Middle Aged<br/>Multiple System Atrophy--complications<br/>Myelin Sheath--pathology<br/>Nerve Degeneration--pathology<br/>Nerve Tissue Proteins--genetics<br/>Neuroglia--metabolism<br/>Nuclear Proteins--genetics<br/>Point Mutation--genetics<br/>Putamen--metabolism<br/>Repressor Proteins--genetics<br/>Severity of Illness Index<br/>Spinocerebellar Ataxias--complications<br/>alpha-Synuclein--genetics