Efficacy of antiseizure medication in a mouse model of HCN1 developmental and epileptic encephalopathy
Author:
Affiliation:
1. Florey Institute of Neuroscience and Mental Health University of Melbourne Parkville Victoria Australia
2. Epilepsy Research Centre, Department of Medicine, University of Melbourne Austin Health Heidelberg Victoria Australia
Funder
Department of Education, Skills and Employment, Australian Government
National Health and Medical Research Council
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/epi.17447
Reference24 articles.
1. De novo mutations in HCN1 cause early infantile epileptic encephalopathy
2. HCN1mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond
3. A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability
4. Genetic characteristics of non-familial epilepsy
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