Brussino, A <br/><br/>
FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia.  [electronic resource] 

 -  Neurology  Jan 2005 
 - 145-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/01.WNL.0000148723.37489.3F  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Age of Onset<br/>Aged<br/>Cerebellar Ataxia--etiology<br/>Fragile X Mental Retardation Protein<br/>Humans<br/>Male<br/>Mutation--genetics<br/>Nerve Tissue Proteins--genetics<br/>RNA-Binding Proteins--genetics<br/>Trinucleotide Repeat Expansion--genetics