Duarri, Anna <br/><br/>
Functional analysis helps to define KCNC3 mutational spectrum in Dutch ataxia cases.  [electronic resource] 

 -  PloS one  2015 
 - e0116599 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1932-6203 
<br/><br/><label>Standard No.: </label>10.1371/journal.pone.0116599  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Computer Simulation<br/>Genetic Association Studies<br/>Genetic Predisposition to Disease<br/>HeLa Cells<br/>Humans<br/>Middle Aged<br/>Mutation<br/>Netherlands<br/>Sequence Analysis, DNA<br/>Shaw Potassium Channels--genetics<br/>Spinocerebellar Ataxias--genetics<br/>White People--genetics<br/>Young Adult