Opening the KV3.1 gates: A therapeutic strategy for progressive myoclonus epilepsy type 7?

Author:

Gandini Maria A.,Zamponi Gerald W.

Publisher

Elsevier BV

Reference8 articles.

1. Targeted therapy improves cellular dysfunction, ataxia, and seizure susceptibility in a model of a progressive myoclonus epilepsy;Feng;Cell Rep. Med.,2024

2. Neurological channelopathies: new insights into disease mechanisms and ion channel function;Kullmann;J. Physiol.,2010

3. Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K(+) channel properties;Oliver;Ann. Neurol.,2017

4. Encephalopathies with KCNC1 variants: genotype-phenotype-functional correlations;Cameron;Ann. Clin. Transl. Neurol.,2019

5. A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy;Muona;Nat. Genet.,2015

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