Kanemasa, Hikaru <br/><br/>
De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis.  [electronic resource] 

 -  BMC neurology  Sep 2016 
 - 174 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1471-2377 
<br/><br/><label>Standard No.: </label>10.1186/s12883-016-0680-6  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Athetosis--complications<br/>Child<br/>Chorea--complications<br/>Hemiplegia--complications<br/>Humans<br/>Male<br/>Mutation<br/>Paralysis--complications<br/>Phenotype<br/>Sodium-Potassium-Exchanging ATPase--genetics