Epilepsy phenotype and response to KCNQ openers in mice harboring the Kcnq2 R207W voltage-sensor mutation
Author:
Publisher
Elsevier BV
Subject
Neurology
Reference42 articles.
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4. Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutation;Blumkin;Eur. J. Paediatr. Neurol.,2012
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3. Altered neurological and neurobehavioral phenotypes in a mouse model of the recurrentKCNB1-p.R306C voltage-sensor variant;2023-03-30
4. Functional characterization and in vitro pharmacological rescue of KCNQ2 pore mutations associated with epileptic encephalopathy;Acta Pharmacologica Sinica;2023-03-17
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