Corbett, Mark A <br/><br/>
Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy.  [electronic resource] 

 -  Neurology  Nov 2016 
 - 1975-1984 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/WNL.0000000000003309  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Animals<br/>Anticonvulsants--therapeutic use<br/>Ataxia--genetics<br/>Child<br/>Child, Preschool<br/>Cohort Studies<br/>DNA Mutational Analysis<br/>Epilepsy--drug therapy<br/>Family Health<br/>Female<br/>Humans<br/>Infant<br/>Kv1.2 Potassium Channel--genetics<br/>Male<br/>Membrane Potentials--genetics<br/>Middle Aged<br/>Models, Chemical<br/>Mutation--genetics<br/>Oocytes<br/>Pharmacogenetics<br/>Xenopus laevis<br/>Young Adult