Mhanni, A A <br/><br/>
Variable expressivity of a novel mutation in the SCN1A gene leading to an autosomal dominant seizure disorder.  [electronic resource] 

 -  Seizure  Nov 2011 
 - 711-2 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1532-2688 
<br/><br/><label>Standard No.: </label>10.1016/j.seizure.2011.06.014  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child, Preschool<br/>Epilepsy--diagnosis<br/>Gene Expression Regulation<br/>Genes, Dominant<br/>Genetic Variation--genetics<br/>Humans<br/>Leucine--genetics<br/>Male<br/>Mutation, Missense--genetics<br/>NAV1.1 Voltage-Gated Sodium Channel<br/>Nerve Tissue Proteins--biosynthesis<br/>Pedigree<br/>Seizures, Febrile--diagnosis<br/>Sodium Channels--biosynthesis<br/>Valine--genetics