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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| Autor principal: | |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Pediatric Neurology Briefs Publishers
2004-05-01
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| coleção: | Pediatric Neurology Briefs |
| Assuntos: | |
| Acesso em linha: | https://www.pediatricneurologybriefs.com/articles/1395 |
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