Manole, Andreea <br/><br/>
De novo KCNA2 mutations cause hereditary spastic paraplegia.  [electronic resource] 

 -  Annals of neurology  02 2017 
 - 326-328 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't; Comment 
<br/><br/><label>ISSN: </label>1531-8249 
<br/><br/><label>Standard No.: </label>10.1002/ana.24866  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Ataxia<br/>Databases, Genetic<br/>Humans<br/>Kv1.2 Potassium Channel<br/>Mutation<br/>Spastic Paraplegia, Hereditary