Distinct phenotypes in zebrafish models of human startle disease()

Startle disease is an inherited neurological disorder that causes affected individuals to suffer noise- or touch-induced non-epileptic seizures, excessive muscle stiffness and neonatal apnea episodes. Mutations known to cause startle disease have been identified in glycine receptor subunit (GLRA1 an...

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Detalles Bibliográficos
Autores principales: Ganser, Lisa R., Yan, Qing, James, Victoria M., Kozol, Robert, Topf, Maya, Harvey, Robert J., Dallman, Julia E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2013
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3972633/
https://www.ncbi.nlm.nih.gov/pubmed/24029548
http://dx.doi.org/10.1016/j.nbd.2013.09.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3972633/
https://www.ncbi.nlm.nih.gov/pubmed/24029548
http://dx.doi.org/10.1016/j.nbd.2013.09.002

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