SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrum.

Herlenius, Eric; Heron, Sarah E; Grinton, Bronwyn E; Keay, Deborah; Scheffer, Ingrid E; Mulley, John C; Berkovic, Samuel F

Herlenius, Eric; Heron, Sarah E; Grinton, Bronwyn E; Keay, Deborah; Scheffer, Ingrid E; Mulley, John C; Berkovic, Samuel F.

Affiliation

Herlenius E; Department of Woman and Child Health, Astrid Lindgren's Children's Hospital, Karolinska Institutet, Stockholm, Sweden.

Epilepsia ; 48(6): 1138-42, 2007 Jun.

Article in En | MEDLINE | ID: mdl-17386050

Subject(s)

Epilepsy, Benign Neonatal/genetics; Mutation/genetics; Nerve Tissue Proteins/genetics; Sodium Channels/genetics; Adolescent; Adult; Age Factors; Age of Onset; Aged; Aged, 80 and over; Australia/epidemiology; Child; DNA Mutational Analysis; Electroencephalography/statistics & numerical data; Epilepsy, Benign Neonatal/diagnosis; Epilepsy, Benign Neonatal/epidemiology; Family; Genetic Carrier Screening; Humans; Infant; Middle Aged; NAV1.2 Voltage-Gated Sodium Channel; Pedigree; Phenotype; Sweden/epidemiology

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Collection: 01-internacional Database: MEDLINE Main subject: Sodium Channels / Epilepsy, Benign Neonatal / Mutation / Nerve Tissue Proteins Type of study: Clinical_trials / Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Aged / Aged80 / Child / Humans / Infant / Middle aged Country/Region as subject: Europa / Oceania Language: En Journal: Epilepsia Year: 2007 Document type: Article Affiliation country: Sweden Country of publication: United States

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