Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutation
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Elsevier BV
Reference19 articles.
1. Neugeborenenkraempfe im Rahmen einer epileptisch belasteten Familie;Rett;Wien Klin Wschr,1964
2. Andreas Rett and benign familial neonatal convulsions revisited;Zimprich;Neurology,2006
3. A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns;Singh;Nat Genet,1998
4. A potassium channel mutation in neonatal human epilepsy;Biervert;Science,1998
5. Functional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsy;Yang;J Biol Chem,1998
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