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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Bibliografiske detaljer

Hovedforfatter:	J Gordon Millichap
Format:	Artigo
Sprog:	Inglês
Udgivet:	Pediatric Neurology Briefs Publishers 2004-05-01
Serier:	Pediatric Neurology Briefs
Fag:	scn2a mutations benign familial neonatal-infantile seizures febrile seizures
Online adgang:	https://www.pediatricneurologybriefs.com/articles/1395
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