A relatively mild phenotype associated with mutation of SCN8A.

Bagnasco, Irene; Dassi, Patrizia; Blé, Roberta; Vigliano, Piernanda

Bagnasco, Irene; Dassi, Patrizia; Blé, Roberta; Vigliano, Piernanda.

Affiliation

Bagnasco I; Division of Child Neuropsychiatry, Martini Hospital, via Tofane 71, 10141 Torino, Italy. Electronic address: irene.bagnasco@aslcittaditorino.it.
Dassi P; Division of Child Neuropsychiatry, Martini Hospital, via Tofane 71, 10141 Torino, Italy.
Blé R; Division of Child Neuropsychiatry, Martini Hospital, via Tofane 71, 10141 Torino, Italy.
Vigliano P; Division of Child Neuropsychiatry, Martini Hospital, via Tofane 71, 10141 Torino, Italy.

Seizure ; 56: 47-49, 2018 Mar.

Article in En | MEDLINE | ID: mdl-29432985

Subject(s)

Epilepsy/genetics; Epilepsy/physiopathology; Mutation/genetics; NAV1.6 Voltage-Gated Sodium Channel/genetics; Brain Waves/genetics; Child; Electroencephalography; Female; Humans; Phenotype

Key words

Infantile benign epilepsy; Movement disorders; Normal cognitive development; SCN8A mutation

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy / NAV1.6 Voltage-Gated Sodium Channel / Mutation Type of study: Risk_factors_studies Limits: Child / Female / Humans Language: En Journal: Seizure Journal subject: NEUROLOGIA Year: 2018 Document type: Article Country of publication: United kingdom

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