Varaico: Literature-Extracted Genetic Variants

Gene:KCNQ3
Variant:p.R230H
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KCNQ3

NM_004519.4:p.R230H

Associated Papers

Electrophysiological Abnormalities and Pharmacological Corrections of Pathogenic Missense Variants in KCNQ3.

Wu X et al.

Neuroscience Bulletin, 2025

Amitriptyline use in individuals with KCNQ2/3 gain-of-function variants: A retrospective cohort study.

De Wachter M et al.

Epilepsia, 2025

A Retrospective Review of Reclassification of Variants of Uncertain Significance in a Pediatric Epilepsy Cohort Undergoing Genetic Panel Testing.

Chourasia N et al.

Pediatric Neurology, 2024

Potassium channel-related epilepsy: Pathogenesis and clinical features.

Zhao T et al.

Epilepsia Open, 2024

KCNQ potassium channels modulate Wnt activity in gastro-oesophageal adenocarcinomas.

Shorthouse D et al.

Life Science Alliance, 2023

37748809 (PubMed )
Supplement: LSA-2023-02124_TableS2.xlsx › Table_S2

Genetic Diagnosis of Children With Neurodevelopmental Disorders Using Whole Genome Sequencing.

Shin S et al.

Pediatric Neurology, 2023

Clinical analysis and functional characterization of KCNQ2-related developmental and epileptic encephalopathy.

Ye J et al.

Frontiers in Molecular Neuroscience, 2023

Characterizing Genotypes and Phenotypes Associated with Dysfunction of Channel-Encoding Genes in a Cohort of Patients with Intellectual Disability.

Ehtesham N et al.

Archives of Iranian Medicine, 2022

Genetic analysis of neurodevelopmental disorders in children.

Wu D et al.

Frontiers in Child and Adolescent Psychiatry, 2022

Autism-associated mutations in KV7 channels induce gating pore current.

Gamal El-Din TM et al.

Proceedings of the National Academy of Sciences of the United States of America, 2021

Flexible Stoichiometry: Implications for KCNQ2- and KCNQ3-Associated Neurodevelopmental Disorders.

Springer K et al.

Developmental Neuroscience, 2021

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.

Wang T et al.

Nature Communications, 2020

33004838 (PubMed )
Supplement: 41467_2020_18723_MOESM11_ESM.xlsx › Supplementary_Data_9

Epileptic channelopathies caused by neuronal Kv7 (KCNQ) channel dysfunction.

Nappi P et al.

Pflugers Archiv : European Journal of Physiology, 2020

Autism and developmental disability caused by KCNQ3 gain-of-function variants.

Sands TT et al.

Annals of Neurology, 2019

Epilepsy-associated mutations in the voltage sensor of KCNQ3 affect voltage dependence of channel opening.

Barro-Soria R

The Journal of General Physiology, 2019

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."