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Modelling human KCNT1-epilepsy in <i>Drosophila</i> : a seizure phenotype and drug responses

2023-04-12

Abstract excerpt

Mutations in the KCNT1 potassium channel cause severe forms of epilepsy which are resistant to current treatments. In vitro studies have shown that KCNT1- epilepsy mutations are gain of function, significantly increasing K + current amplitudes. To investigate if Drosophila can be used to model human KCNT1 epilepsy, we generated Drosophila melanogaster lines carrying human KCNT1 with the patient mutation G2...

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Literature Corpus work
4e2f5ca4-db47-51d3-bbab-547f96b510e6
DOI
10.1101/2023.04.11.536495
Open publication

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Modelling human KCNT1-epilepsy in <i>Drosophila</i> : a seizure phenotype and drug responsesDOI 10.1101/2023.04.11.536495
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