Incidence of Dravet Syndrome in a US Population

OBJECTIVE: De novo mutations of the gene sodium channel 1α (SCN1A) are the major cause of Dravet syndrome, an infantile epileptic encephalopathy. US incidence of DS has been estimated at 1 in 40 000, but no US epidemiologic studies have been performed since the advent of genetic testing. METHODS: In...

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Detalhes bibliográficos
Publicado no:Pediatrics
Main Authors: Wu, Yvonne W., Sullivan, Joseph, McDaniel, Sharon S., Meisler, Miriam H., Walsh, Eileen M., Li, Sherian Xu, Kuzniewicz, Michael W.
Formato: Artigo
Idioma:Inglês
Publicado em: American Academy of Pediatrics 2015
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4621800/
https://ncbi.nlm.nih.gov/pubmed/26438699
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1542/peds.2015-1807
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