Jurkat-Rott, K <br/><br/>
Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants.  [electronic resource] 

 -  Neurology  May 2004 
 - 1857-61 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/01.wnl.0000127310.11526.fd  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Amino Acid Sequence<br/>Amino Acid Substitution<br/>Coma--genetics<br/>DNA Mutational Analysis<br/>Epilepsy--genetics<br/>Female<br/>Genetic Predisposition to Disease<br/>Genotype<br/>Hemiplegia--enzymology<br/>Humans<br/>Intellectual Disability--genetics<br/>Male<br/>Middle Aged<br/>Migraine Disorders--enzymology<br/>Models, Molecular<br/>Molecular Sequence Data<br/>Mutation, Missense<br/>Penetrance<br/>Phenotype<br/>Point Mutation<br/>Recurrence<br/>Sequence Alignment<br/>Sequence Homology, Amino Acid<br/>Sodium-Potassium-Exchanging ATPase--chemistry