Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutation
Autor: | Blumkin, Lubov, Suls, Arvid, Deconinck, Tine, De Jonghe, Peter, Linder, Ilan, Kivity, Sara, Dabby, Ron, Leshinsky-Silver, Esther, Lev, Dorit, Lerman-Sagie, Tally |
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Zdroj: | In European Journal of Paediatric Neurology July 2012 16(4):356-360 |
Databáze: | ScienceDirect |
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