SCN2A Mutations and Benign Familial Neonatal-Infantile Seizures

Authors

  • J Gordon Millichap Northwestern University Feinberg School of Medicine

DOI:

https://doi.org/10.15844/pedneurbriefs-18-5-2

Keywords:

SCN2A Mutations, Benign Familial Neonatal-Infantile Seizures, Febrile Seizures

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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Published

2004-05-01

Issue

Vol 18, No 05 | May 2004

Section

Seizure Disorders

License

Copyright (c) 2004 The Author(s)

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