Kaunisto, M A <br/><br/>
A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2.  [electronic resource] 

 -  Neurogenetics  Jun 2004 
 - 141-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1364-6745 
<br/><br/><label>Standard No.: </label>10.1007/s10048-004-0178-z  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Chromosomes, Human, Pair 1<br/>Family Health<br/>Female<br/>Finland<br/>Gene Frequency<br/>Genetic Linkage<br/>Haplotypes<br/>Hemiplegia--genetics<br/>Humans<br/>Male<br/>Migraine Disorders--genetics<br/>Molecular Sequence Data<br/>Mutation, Missense<br/>Pedigree<br/>Sodium-Potassium-Exchanging ATPase--genetics