Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome
Work
Year: 2012
Type: article
Abstract: Dravet syndrome is a severe infantile onset epileptic encephalopathy associated with mutations in the sodium channel alpha 1 subunit gene SCN1A. To date no large studies have systematically examined t... more
Source: Brain
Institutions University of Glasgow, Royal Hospital for Children
Cites: 48
Cited by: 325
Related to: 10
FWCI: 13.17
Citation percentile (by year/subfield): 99.99
Subfield: Psychiatry and Mental health
Field: Medicine
Domain: Health Sciences
Sustainable Development Goal Good health and well-being
Open Access status: bronze