KCNQ2 Encephalopathy and Neonatal Seizures
DOI:
https://doi.org/10.15844/pedneurbriefs-25-11-5Keywords:
KCNQ2 Encephalopathy, Refractory Neonatal Seizures, Heterozygous KCNQ2 MutationsAbstract
Researchers from centers in Belgium and Australia analyzed 80 patients with unexplained neonatal or early infantile seizures and associated psychomotor retardation for KCNQ2 mutations.Published
2011-11-01
Issue
Section
Infectious/Autoimmune Disorders
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