Carregant...

ALLN rescues an in vitro excitatory synaptic transmission deficit in Lis1 mutant mice

LIS1 gene mutations lead to a rare neurological disorder, classical lissencephaly, characterized by brain malformations, mental retardation, seizures, and premature death. Mice heterozygous for Lis1 (Lis1(+/−)) exhibit cortical malformations, defects in neuronal migration, increased glutamate-mediat...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Sebe, Joy Y., Bershteyn, Marina, Hirotsune, Shinji, Wynshaw-Boris, Anthony, Baraban, Scott C.
Format: Artigo
Idioma:Inglês
Publicat: American Physiological Society 2013
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3545457/
https://ncbi.nlm.nih.gov/pubmed/23100132
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/jn.00431.2012
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!