SCN2A Mutations and Benign Familial Neonatal-Infantile Seizures

SCN2A Mutations and Benign Familial Neonatal-Infantile Seizures

SCN2A sodium channel gene was analyzed in 2 families with probable benign familial neonatal-infantile seizures (BFNISs), 9 with possible BFNIS, 10 with benign familial infantile seizures, and in 93 additional families with various early childhood epilepsies, in a study at the University of Melbourne...

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Bibliographic Details
Main Author: J Gordon Millichap
Format: Article
Language:English
Published: Pediatric Neurology Briefs Publishers 2004-05-01
Series:Pediatric Neurology Briefs
Subjects:
scn2a mutations
benign familial neonatal-infantile seizures
febrile seizures
Online Access:https://www.pediatricneurologybriefs.com/articles/1395
Description
Summary:SCN2A sodium channel gene was analyzed in 2 families with probable benign familial neonatal-infantile seizures (BFNISs), 9 with possible BFNIS, 10 with benign familial infantile seizures, and in 93 additional families with various early childhood epilepsies, in a study at the University of Melbourne, Australia, and other international centers.
ISSN:1043-3155
2166-6482

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