Marzin, Pauline <br/><br/>
Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations.  [electronic resource] 

 -  Brain & development  Oct 2018 
 - 768-774 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Video-Audio Media 
<br/><br/><label>ISSN: </label>1872-7131 
<br/><br/><label>Standard No.: </label>10.1016/j.braindev.2018.05.008  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Brain--physiopathology<br/>Child<br/>Child, Preschool<br/>Epilepsy--diagnosis<br/>Female<br/>Hemiplegia--genetics<br/>Humans<br/>Male<br/>Movement Disorders--diagnosis<br/>Mutation<br/>Seizures--diagnosis<br/>Sodium-Potassium-Exchanging ATPase--genetics