Enhanced slow inactivation contributes to dysfunction of a recurrent SCN2A mutation associated with developmental and epileptic encephalopathy
Author:
Affiliation:
1. Department of Pharmacology Northwestern University Feinberg School of Medicine Chicago IL USA
Publisher
Wiley
Subject
Physiology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1113/JP281834
Reference47 articles.
1. De novo mutations in epileptic encephalopathies
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4. Benign familial neonatal-infantile seizures: Characterization of a new sodium channelopathy
5. Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1
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