Ohmori, Iori <br/><br/>
Rasmussen encephalitis associated with SCN 1 A mutation.  [electronic resource] 

 -  Epilepsia  Mar 2008 
 - 521-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0013-9580 
<br/><br/><label>Standard No.: </label>10.1111/j.1528-1167.2007.01411.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>DNA Mutational Analysis<br/>Electroencephalography--statistics & numerical data<br/>Encephalitis--diagnosis<br/>Epilepsies, Partial--diagnosis<br/>Female<br/>Genetic Predisposition to Disease--genetics<br/>Humans<br/>Magnetic Resonance Imaging--statistics & numerical data<br/>Membrane Potentials--genetics<br/>Mutation--genetics<br/>NAV1.1 Voltage-Gated Sodium Channel<br/>Nerve Tissue Proteins--genetics<br/>Neurons--physiology<br/>Patch-Clamp Techniques<br/>Pedigree<br/>Phenotype<br/>Sodium Channels--genetics<br/>Synaptic Transmission--genetics<br/>Syndrome<br/>Tomography, Emission-Computed, Single-Photon