Associated Papers
Electrophysiological Abnormalities and Pharmacological Corrections of Pathogenic Missense Variants in KCNQ3.
Wu X et al.
Neuroscience Bulletin, 2025
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
Wang T et al.
Nature Communications, 2020
33004838 (PubMed )
Supplement: 41467_2020_18723_MOESM16_ESM.xlsx › Supplementary_Data_14_-_KCNQ3
A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability.
Miceli F et al.
Epilepsia, 2015
Sodium and potassium channel dysfunctions in rare and common idiopathic epilepsy syndromes.
Hahn A et al.
Brain & Development, 2009
KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes.
Neubauer BA et al.
Neurology, 2008
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