Associated Papers
Electrophysiological Abnormalities and Pharmacological Corrections of Pathogenic Missense Variants in KCNQ3.
Wu X et al.
Neuroscience Bulletin, 2025
Benign familial infantile epilepsy associated with KCNQ3 mutation: a rare occurrence or an underestimated event?
Nardello R et al.
Epileptic Disorders : International Epilepsy Journal With Videotape, 2020
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
Wang T et al.
Nature Communications, 2020
33004838 (PubMed )
Supplement: 41467_2020_18723_MOESM5_ESM.xlsx › Supplementary_Data_3
Select a paper to view details