Yabe, Ichiro <br/><br/>
Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma.  [electronic resource] 

 -  Archives of neurology  Dec 2003 
 - 1749-51 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0003-9942 
<br/><br/><label>Standard No.: </label>10.1001/archneur.60.12.1749  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Arginine<br/>Base Sequence--genetics<br/>Case-Control Studies<br/>Glycine<br/>Heterozygote<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation, Missense<br/>Pedigree<br/>Protein Kinase C--genetics<br/>Spinocerebellar Ataxias--classification