Spectrum of SCN8A-Related Epilepsy
Investigators from the EuroEPINOMICS European research consortium studied 17 patients with epileptic encephalopathy due to SCN8A mutations and reported the specific genetic and phenotypic features
Veröffentlicht in: | Pediatric neurology briefs. - 1997. - 29(2015), 2 vom: 01. Feb., Seite 16 |
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Format: | Online-Aufsatz |
Sprache: | English |
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2015
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Zugriff auf das übergeordnete Werk: | Pediatric neurology briefs |
Schlagworte: | Journal Article Dravet Syndrome Epileptic Encephalopathies SCN8A Voltage Gated Sodium Channels |
Zusammenfassung: | Investigators from the EuroEPINOMICS European research consortium studied 17 patients with epileptic encephalopathy due to SCN8A mutations and reported the specific genetic and phenotypic features |
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Beschreibung: | Date Completed 02.03.2016 Date Revised 29.09.2020 published: Print Citation Status PubMed-not-MEDLINE |
ISSN: | 1043-3155 |
DOI: | 10.15844/pedneurbriefs-29-2-7 |