Duplication of the sodium channel gene cluster on 2q24 in children with early onset epilepsy

An interstitial duplication at 2q24.3 involving the SCN1A, SCN2A, SCN3A genes associated with infantile epilepsy

(2011) Gerald Raymond et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Refractory neonatal epilepsy with a de novo duplication of chromosome 2q24.2q24.3

(2011) Akihisa Okumura et al.   EPILEPSIA

The genetics of Dravet syndrome

(2011) Carla Marini et al.   EPILEPSIA

Infantile epilepsy associated with mosaic 2q24 duplication including SCN2A and SCN3A

(2011) Marilena Vecchi et al.   SEIZURE-EUROPEAN JOURNAL OF EPILEPSY

Epilepsies and epileptic syndromes starting in the neonatal period

(2010) Hitoshi Yamamoto et al.   BRAIN & DEVELOPMENT

Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3

(2010) Sarah E. Heron et al.   EPILEPSIA

SCN1Aduplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis

(2009) Carla Marini et al.   EPILEPSIA

Genetics of epilepsy syndromes starting in the first year of life

(2009) L. Deprez et al.   NEUROLOGY

Newly diagnosed single unprovoked seizures and epilepsy in Stockholm, Sweden: First report from the Stockholm Incidence Registry of Epilepsy (SIRE)

(2008) Cecilia Adelöw et al.   EPILEPSIA

Epilepsy and electroencephalographic anomalies in chromosome 2 aberrations

(2008) Salvatore Grosso et al.   EPILEPSY RESEARCH

Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsy

(2008) Katherine D. Holland et al.   NEUROSCIENCE LETTERS