De novo SCN2A splice site mutation in a boy with Autism spectrum disorder

Early sensory over-responsivity in toddlers with autism spectrum disorders as a predictor of family impairment and parenting stress

(2013) A. Ben-Sasson et al.   JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY

Clinical spectrum of SCN2A mutations expanding to Ohtahara syndrome

(2013) K. Nakamura et al.   NEUROLOGY

Major channels involved in neuropsychiatric disorders and therapeutic perspectives

(2013) Paola Imbrici et al.   Frontiers in Genetics

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

(2012) Barbara Goeggel Simonetti et al.   EPILEPSIA

Patterns and rates of exonic de novo mutations in autism spectrum disorders

(2012) Benjamin M. Neale et al.   NATURE

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

(2012) Stephan J. Sanders et al.   NATURE

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

MosaicSCN1Amutations in familial partial epilepsy with antecedent febrile seizures

(2011) Y.-W. Shi et al.   GENES BRAIN AND BEHAVIOR

Disruption of the SCN2A and SCN3A genes in a patient with mental retardation, neurobehavioral and psychiatric abnormalities, and a history of infantile seizures

(2010) M Bartnik et al.   CLINICAL GENETICS

Advances in autism genetics: on the threshold of a new neurobiology

(2008) Brett S. Abrahams et al.   NATURE REVIEWS GENETICS