SCN1A mutational analysis in Korean patients with Dravet syndrome

Seizure

Volumn 20, Issue 10, 2011, Pages 789-794

  Lim, Byung Chan ^a   Hwang, Hee ^a   Chae, Jong Hee ^a   Choi, Ji Eun ^a   Hwang, Yong Seung ^a   Kang, Seong Ho ^b   Ki, Chang Seok ^c   Kim, Ki Joong ^a  

^a Seoul National University Children's Hospital   (South Korea)

^b Green Cross Reference Laboratory   (South Korea)

^c Sungkyunkwan University School of Medicine   (South Korea)

Author keywords

Dravet syndrome; Korea; SCN1A

Indexed keywords

CLOBAZAM; CLONAZEPAM; ETIRACETAM; LAMOTRIGINE; RUFINAMIDE; SODIUM CHANNEL NAV1.1; TOPIRAMATE; VALPROIC ACID; ZONISAMIDE;

ABSENCE; ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; EXON; FRAMESHIFT MUTATION; GRAND MAL SEIZURE; HUMAN; KOREA; MISSENSE MUTATION; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; MUTATIONAL ANALYSIS; MYOCLONUS SEIZURE; NONSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; SEVERE MYOCLONIC EPILEPSY IN INFANCY; TONIC CLONIC SEIZURE;

AGE OF ONSET; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; EPILEPSY; FEMALE; HUMANS; INFANT; MALE; MULTIPLEX POLYMERASE CHAIN REACTION; NERVE TISSUE PROTEINS; PEDIGREE; SODIUM CHANNELS;

EID: 84860406836     PISSN: 10591311     EISSN: 15322688     Source Type: Journal    
DOI: 10.1016/j.seizure.2011.08.002     Document Type: Article

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