Pediatric Neurology Briefs
Published 2004 | Version v1.0.0
Journal Article Open

SCN2A Mutations and Benign Familial Neonatal-Infantile Seizures

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Abstract

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.

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PNB-18-34

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Created
2004
When the item was originally created.