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
Publié dans: | Pediatric neurology briefs. - 1997. - 29(2015), 2 vom: 01. Feb., Seite 16 |
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Auteur principal: | |
Autres auteurs: | |
Format: | Article en ligne |
Langue: | English |
Publié: |
2015
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Accès à la collection: | Pediatric neurology briefs |
Sujets: | Journal Article Dravet Syndrome Epileptic Encephalopathies SCN8A Voltage Gated Sodium Channels |
Accès en ligne |
Volltext |