Duarri, Anna <br/><br/>
Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant manner.  [electronic resource] 

 -  Cellular and molecular life sciences : CMLS  Sep 2015 
 - 3387-99 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1420-9071 
<br/><br/><label>Standard No.: </label>10.1007/s00018-015-1894-2  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Analysis of Variance<br/>Cycloheximide<br/>DNA Primers--genetics<br/>HeLa Cells<br/>Humans<br/>Image Processing, Computer-Assisted<br/>Immunohistochemistry<br/>Mutagenesis, Site-Directed<br/>Mutation--genetics<br/>Purkinje Cells--metabolism<br/>Shal Potassium Channels--genetics<br/>Spinocerebellar Degenerations--genetics