The epilepsy phenotype of KCNK4-related neurodevelopmental disease

Author:

Krygier MagdalenaORCID,Ziętkiewicz SzymonORCID,Talaśka-Liczbik Weronika,Chylińska MagdalenaORCID,Walczak Anna,Kostrzewa Grażyna,Płoski RafałORCID,Mazurkiewicz-Bełdzińska Maria

Publisher

Elsevier BV

Reference39 articles.

1. From genetictesting to precision medicine in epilepsy;Striano;Neurotherapeutics,2020

2. IonChannels in geneticepilepsy: from genes and mechanisms to disease-TargetedTherapies;Oyrer;PharmacolRev,2018

3. Potassium channel-relatedepilepsy: pathogenesis and clinicalfeatures;Zhao;Epilepsia Open,2024

4. Much morethan a leak: structure and function of K₂p-channels;Renigunta;Pflugers Arch,2015

5. Mutations in KCNK4 thatAffectGatingCause a RecognizableNeurodevelopmentalSyndrome;Bauer;Am J Hum Genet,2018

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