Proteomic signature of the Dravet syndrome in the genetic Scn1a-A1783V mouse model

Proteomic signature of the Dravet syndrome in the genetic Scn1a-A1783V mouse model

Background: Dravet syndrome is a rare, severe pediatric epileptic encephalopathy associated with intellectual and motor disabilities. Proteomic profiling in a mouse model of Dravet syndrome can provide information about the molecular consequences of the genetic deficiency and about pathophysiologica...

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Bibliographic Details
Main Authors: Nina Miljanovic, Stefanie M. Hauck, R. Maarten van Dijk, Valentina Di Liberto, Ali Rezaei, Heidrun Potschka
Format: Article
Language:English
Published: Elsevier 2021-09-01
Series:Neurobiology of Disease
Subjects:
Proteome
Genetic epilepsy
Epileptic encephalopathy
Scn1a
Mice
Online Access:http://www.sciencedirect.com/science/article/pii/S0969996121001728

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http://www.sciencedirect.com/science/article/pii/S0969996121001728

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