van de Warrenburg, B P C <br/><br/>
Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family.  [electronic resource] 

 -  Neurology  Dec 2003 
 - 1760-5 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.0000098883.79421.73  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Age of Onset<br/>Aged<br/>Aged, 80 and over<br/>Cerebellar Ataxia--diagnosis<br/>Chromosomes, Human, Pair 19--genetics<br/>DNA Mutational Analysis<br/>Exons--genetics<br/>Female<br/>Genes, Dominant<br/>Genetic Linkage<br/>Haplotypes<br/>Humans<br/>Magnetic Resonance Imaging<br/>Male<br/>Middle Aged<br/>Mutation, Missense<br/>Netherlands--epidemiology<br/>Pedigree<br/>Protein Kinase C--genetics