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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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
2004-05-01
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| Series: | Pediatric Neurology Briefs |
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| Online Access: | https://www.pediatricneurologybriefs.com/articles/1395 |