Varaico: Literature-Extracted Genetic Variants

Gene:KCNA1
Variant:p.R307C
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KCNA1

NM_000217.3:p.R307C

Associated Papers

A conifer metabolite corrects episodic ataxia type 1 by voltage sensor-mediated ligand activation of Kv1.1.

Manville RW et al.

Proceedings of the National Academy of Sciences of the United States of America, 2025

Novel Genetic Variants Expand the Functional, Molecular, and Pathological Diversity of KCNA1 Channelopathy.

Paulhus K et al.

International Journal of Molecular Sciences, 2023

Case report: A novel loss-of-function pathogenic variant in the KCNA1 cytoplasmic N-terminus causing carbamazepine-responsive type 1 episodic ataxia.

Manville RW et al.

Frontiers in Neurology, 2022

Therapeutic Potential of Sodium Channel Blockers as a Targeted Therapy Approach in KCNA1-Associated Episodic Ataxia and a Comprehensive Review of the Literature.

Lauxmann S et al.

Frontiers in Neurology, 2021

Two novel KCNA1 variants identified in two unrelated Chinese families affected by episodic ataxia type 1 and neurodevelopmental disorders.

Yuan H et al.

Molecular Genetics & Genomic Medicine, 2020

Kv1.1 Channelopathies: Pathophysiological Mechanisms and Therapeutic Approaches.

D'Adamo MC et al.

International Journal of Molecular Sciences, 2020

Clinical Spectrum of KCNA1 Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity.

Paulhus K et al.

International Journal of Molecular Sciences, 2020

Complete loss of KCNA1 activity causes neonatal epileptic encephalopathy and dyskinesia.

Verdura E et al.

Journal of Medical Genetics, 2020

New insights into the pathogenesis and therapeutics of episodic ataxia type 1.

D'Adamo MC et al.

Frontiers in Cellular Neuroscience, 2015

Episodic ataxia type 1: clinical characterization, quality of life and genotype-phenotype correlation.

Graves TD et al.

Brain : a Journal of Neurology, 2014

Characterization of the Kv1.1 I262T and S342I mutations associated with episodic ataxia 1 with distinct phenotypes.

Zhu J et al.

Archives of Biochemistry and Biophysics, 2012

Nongenetic factors influence severity of episodic ataxia type 1 in monozygotic twins.

Graves TD et al.

Neurology, 2010

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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."