Varaico: Literature-Extracted Genetic Variants

Gene:HCN2
Variant:p.F738C
Back to variants list

HCN2

NM_001194.4:p.F738C

Associated Papers

The Contribution of HCN Channelopathies in Different Epileptic Syndromes, Mechanisms, Modulators, and Potential Treatment Targets: A Systematic Review.

Kessi M et al.

Frontiers in Molecular Neuroscience, 2022

Are Variants Causing Cardiac Arrhythmia Risk Factors in Sudden Unexpected Death in Epilepsy?

Bleakley LE et al.

Frontiers in Neurology, 2020

Genetic Basis of Sudden Unexpected Death in Epilepsy.

Bagnall RD et al.

Frontiers in Neurology, 2017

Genetic analysis of hyperpolarization-activated cyclic nucleotide-gated cation channels in sudden unexpected death in epilepsy cases.

Tu E et al.

Brain Pathology (zurich, Switzerland), 2011

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

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."