Targeted therapy improves cellular dysfunction, ataxia, and seizure susceptibility in a model of a progressive myoclonus epilepsy
Author:
Publisher
Elsevier BV
Subject
General Biochemistry, Genetics and Molecular Biology
Reference63 articles.
1. Myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK) is caused by heterozygous KCNC1 mutations;Nascimento;Epileptic Disord.,2016
2. A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy;Muona;Nat. Genet.,2015
3. Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K(+) channel properties;Oliver;Ann. Neurol.,2017
4. Progressive Myoclonus Epilepsies;Kälviäinen;Semin. Neurol.,2015
5. The best evidence for progressive myoclonic epilepsy: A pathway to precision therapy;Orsini;Seizure,2019
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