Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel α1 subunit gene, SCN1A

Epilepsy Research

Volumn 48, Issue 1-2, 2002, Pages 15-23

  Ito, M ^a   Nagafuji, H ^b   Okazawa, H ^c   Yamakawa, K ^d   Sugawara, T ^d   Mazaki Miyazaki, E ^d   Hirose, S ^e   Fukuma, G ^e   Mitsudome, A ^e   Wada, K ^f   Kaneko, S ^f  

^a SHIGA MEDICAL CENTER FOR CHILDREN   (Japan)

^b Kitano Hospital   (Japan)

^c SHIGA MEDICAL CENTER FOR ADULTS   (Japan)

^d RIKEN BRAIN SCIENCE INSTITUTE   (Japan)

^e FUKUOKA UNIVERSITY   (Japan)

^f HIROSAKI UNIVERSITY   (Japan)

Author keywords

Autosomal dominant; Epilepsy; Febrile seizure; Na+ channel; Partial epilepsy; Severe myoclonic epilepsy of infancy

Indexed keywords

SODIUM CHANNEL;

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; ELECTROENCEPHALOGRAPHY; EPILEPSY; FAMILY; FEBRILE CONVULSION; FEMALE; FOCAL EPILEPSY; GENE; GENE MUTATION; GENERALIZED EPILEPSY; GENETIC DISORDER; GRAND MAL EPILEPSY; HUMAN; JAPAN; MALE; MISSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; SCN1A GENE;

ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOME DISORDERS; ELECTROENCEPHALOGRAPHY; EPILEPSY; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION, MISSENSE; NERVE TISSUE PROTEINS; PEDIGREE; SEIZURES, FEBRILE; SODIUM CHANNELS;

EID: 0036158906     PISSN: 09201211     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0920-1211(01)00313-8     Document Type: Article

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