Costa, Cinzia <br/><br/>
A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy.  [electronic resource] 

 -  Cephalalgia : an international journal of headache  Jan 2014 
 - 68-72 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1468-2982 
<br/><br/><label>Standard No.: </label>10.1177/0333102413498941  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Epilepsy--diagnosis<br/>Female<br/>Genetic Predisposition to Disease--genetics<br/>Hemiplegia--diagnosis<br/>Humans<br/>Male<br/>Middle Aged<br/>Migraine Disorders--diagnosis<br/>Mutation--genetics<br/>Polymorphism, Single Nucleotide--genetics<br/>Sodium-Potassium-Exchanging ATPase--genetics