Nav1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome

Adults with a history of possible Dravet syndrome: An illustration of the importance of analysis of the SCN1A gene

(2011) Nienke E. Verbeek et al.   EPILEPSIA

Altered Function of theSCN1AVoltage-gated Sodium Channel Leads to γ-Aminobutyric Acid-ergic (GABAergic) Interneuron Abnormalities

(2010) Melinda S. Martin et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

NaV1.1 channels and epilepsy

(2010) William A. Catterall et al.   JOURNAL OF PHYSIOLOGY-LONDON

Milder phenotype with SCN1A truncation mutation other than SMEI

(2010) Mei-Juan Yu et al.   SEIZURE-EUROPEAN JOURNAL OF EPILEPSY

A Functional Null Mutation of SCN1B in a Patient with Dravet Syndrome

(2009) G. A. Patino et al.   JOURNAL OF NEUROSCIENCE

Temperature- and age-dependent seizures in a mouse model of severe myoclonic epilepsy in infancy

(2009) J. C. Oakley et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

A catalog of SCN1A variants

(2008) Christoph Lossin   BRAIN & DEVELOPMENT

Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients

(2008) C Depienne et al.   JOURNAL OF MEDICAL GENETICS