De Cunto, Angela <br/><br/>
A case of familial hemiplegic migraine associated with a novel ATP1A2 gene mutation.  [electronic resource] 

 -  Pediatric neurology  Aug 2012 
 - 133-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1873-5150 
<br/><br/><label>Standard No.: </label>10.1016/j.pediatrneurol.2012.04.012  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Child, Preschool<br/>Humans<br/>Male<br/>Migraine with Aura--diagnosis<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Pedigree<br/>Sodium-Potassium-Exchanging ATPase--genetics