Original paper

Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability

Brain10.60
Volume: 142, Issue: 2, Pages: 376 - 390
Published: Jan 4, 2019
Abstract
Ion channel mutations can cause distinct neuropsychiatric diseases. We first studied the biophysical and neurophysiological consequences of four mutations in the human Na+ channel gene SCN8A causing either mild (E1483K) or severe epilepsy (R1872W), or intellectual disability and autism without epilepsy (R1620L, A1622D). Only combined electrophysiological recordings of transfected wild-type or mutant channels in both neuroblastoma cells and...
Paper Details
Title
Neuronal mechanisms of mutations in SCN8A causing epilepsy or intellectual disability
Published Date
Jan 4, 2019
Journal
Volume
142
Issue
2
Pages
376 - 390
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