Cargando…
Photosensitivity and CHD2 Variants
Investigators from multinational institutions hypothesized that disruption of CHD2, which encodes chromodomain helicase DNA-binding protein 2, would be associated with common forms of photosensitive epilepsy or photosensitivity manifesting as a photoparoxysmal response alone.
Autores principales: | Sosa, Rebecca García, Nangia, Srishti |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pediatric Neurology Briefs Publishers
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4747278/ https://www.ncbi.nlm.nih.gov/pubmed/26933602 http://dx.doi.org/10.15844/pedneurbriefs-29-9-1 |
Ejemplares similares
-
Phenotypes of Dravet Syndrome
por: Garcia-Sosa, Rebecca, et al.
Publicado: (2016) -
KCNA2-Related Epileptic Encephalopathy
por: Kearney, Jennifer A.
Publicado: (2015) -
Understanding the Spectrum of SLC2A1-Associated Disorders
por: Fajardo, Marytery, et al.
Publicado: (2017) -
Incidence of Dravet Syndrome in a US Population
por: Krueger, Jena, et al.
Publicado: (2015) -
Prognosis with Incidental Rolandic Spikes
por: Gertler, Tracy S., et al.
Publicado: (2015)