Fine Mapping of a Dravet Syndrome Modifier Locus on Mouse Chromosome 5 and Candidate Gene Analysis by RNA-Seq

A substantial number of mutations have been identified in voltage-gated sodium channel genes that result in various forms of human epilepsy. SCN1A mutations result in a spectrum of severity ranging from mild febrile seizures to Dravet syndrome, an infant-onset epileptic encephalopathy. Dravet syndro...

Descripción completa

Detalles Bibliográficos
Autores principales: Hawkins, Nicole A., Zachwieja, Nicole J., Miller, Alison R., Anderson, Lyndsey L., Kearney, Jennifer A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074504/
https://www.ncbi.nlm.nih.gov/pubmed/27768696
http://dx.doi.org/10.1371/journal.pgen.1006398

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074504/
https://www.ncbi.nlm.nih.gov/pubmed/27768696
http://dx.doi.org/10.1371/journal.pgen.1006398

Ejemplares similares