Novel de novo SCN2A mutation in a child with migrating focal seizures of infancy

Pediatric Neurology

Volumn 49, Issue 6, 2013, Pages 486-488

  Dhamija, Radhika ^a   Wirrell, Elaine ^a   Falcao, Germano ^b   Kirmani, Salman ^a   Wong Kisiel, Lily C ^a  

^a MAYO CLINIC   (United States)

^b Avera Health   (United States)

Author keywords

migrating focal seizures of infancy; SCN2A gene

Indexed keywords

ASPARTIC ACID; CLOBAZAM; CLONAZEPAM; ETIRACETAM; OXCARBAZEPINE; PHENOBARBITAL; PHENYTOIN; PYRIDOXAMINE PHOSPHATE OXIDASE; PYRIDOXINE; STIRIPENTOL; TOPIRAMATE; VALINE; VIGABATRIN; ZONISAMIDE;

ARTICLE; CASE REPORT; ELECTROENCEPHALOGRAPHY; EPILEPTIC STATE; FEMALE; FOCAL EPILEPSY; GENE; HUMAN; INFANT; INFANT DISEASE; KETOGENIC DIET; MEDICAL HISTORY; MICROARRAY ANALYSIS; MIGRATING FOCAL SEIZURES OF INFANCY; MISSENSE MUTATION; PRIORITY JOURNAL; SODIUM CHANNEL NAV1.2 GENE;

MIGRATING FOCAL SEIZURES OF INFANCY; SCN2A GENE;

DNA MUTATIONAL ANALYSIS; ELECTROENCEPHALOGRAPHY; FEMALE; HUMANS; INFANT; MUTATION; NAV1.2 VOLTAGE-GATED SODIUM CHANNEL; SEIZURES;

EID: 84888250324     PISSN: 08878994     EISSN: 18735150     Source Type: Journal    
DOI: 10.1016/j.pediatrneurol.2013.07.004     Document Type: Article

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