SCN3A deficiency associated with increased seizure susceptibility
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Published:2017-06
Issue:
Volume:102
Page:38-48
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ISSN:0969-9961
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Container-title:Neurobiology of Disease
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language:en
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Short-container-title:Neurobiology of Disease
Author:
Lamar Tyra,
Vanoye Carlos G.,
Calhoun JeffreyORCID,
Wong Jennifer C.,
Dutton Stacey B.B.,
Jorge Benjamin S.,
Velinov Milen,
Escayg Andrew,
Kearney Jennifer A.
Funder
NIH
CCSG
Avon Foundation
Reference61 articles.
1. Exome sequencing identifies a de novo SCN2A mutation in a patient with intractable seizures, severe intellectual disability, optic atrophy, muscular hypotonia, and brain abnormalities;Baasch;Epilepsia,2014
2. Pharmacological characterization of the 6Hz psychomotor seizure model of partial epilepsy;Barton;Epilepsy Res.,2001
3. Rescuable folding defective NaV1.1 (SCN1A) mutants in epilepsy: properties, occurrence, and novel rescuing strategy with peptides targeted to the endoplasmic reticulum;Bechi;Neurobiol. Dis.,2015
4. Differential regulation of three sodium channel messenger RNAs in the rat central nervous system during development;Beckh;EMBO J.,1989
5. Sodium channel mRNAs I, II and III in the CNS: cell-specific expression;Black;Brain Res. Mol. Brain Res.,1994
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