Chromatogram of 453delC mutation in the KCNH2 gene (A) and schematic... | Download Scientific Diagram
Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing | Revista Española de Cardiología
Overexpression KCNH2-3.1 potassium channel is associated with neuronal... | Download Scientific Diagram
A diagram of the Kv11.1 channel trafficking pathway. KCNH2 is... | Download Scientific Diagram
Prolonged QT interval on ECG caused by hERG channel dysfunction.... | Download Scientific Diagram
Heterozygous KCNH2 variant phenotyping using Flp-In HEK293 and high-throughput automated patch clamp electrophysiology | bioRxiv
Genes | Free Full-Text | Analysis of CACNA1C and KCNH2 Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia
Current pharmacogenomic studies on hERG potassium channels: Trends in Molecular Medicine
Cardiac channelopathies: it's in the genes | Nature Medicine
Isogenic human pluripotent stem cell pairs reveal the role of a KCNH2 mutation in long‐QT syndrome | The EMBO Journal
Large-scale mutational analysis of Kv11.1 reveals molecular insights into type 2 long QT syndrome | Nature Communications
Molecular pathogenesis of long QT syndrome type 2 - ScienceDirect
Generation of hiPSCs from a patient with type-2 long-QT syndrome. (A)... | Download Scientific Diagram
The novel frameshift mutation. Sequencing analysis of KCNH2 gene in the... | Download Scientific Diagram
Suppression and Replacement Gene Therapy for KCNH2-Mediated Arrhythmias | Circulation: Genomic and Precision Medicine
Suppression and Replacement Gene Therapy for KCNH2-Mediated Arrhythmias | Circulation: Genomic and Precision Medicine
IJMS | Free Full-Text | Structural Modelling of KCNQ1 and KCNH2 Double Mutant Proteins, Identified in Two Severe Long QT Syndrome Cases, Reveals New Insights into Cardiac Channelopathies
Identification of a novel pathogenic variant in KCNH2 in an Iranian family with long QT syndrome 2 by whole‐exome sequencing - Fazelifar - 2023 - Journal of Arrhythmia - Wiley Online Library
Suppression and Replacement Gene Therapy for KCNH2-Mediated Arrhythmias | Circulation: Genomic and Precision Medicine
Isogenic Sets of hiPSC-CMs Harboring Distinct KCNH2 Mutations Differ Functionally and in Susceptibility to Drug-Induced Arrhythmias - ScienceDirect
Cellular properties of C-terminal KCNH2 long QT syndrome mutations: description and divergence from clinical phenotypes. | Semantic Scholar
Novel mutation in the KCNH2 gene associated with long QT syndrome | Revista Portuguesa de Cardiologia (English edition)
KCNH2 Gene - GeneCards | KCNH2 Protein | KCNH2 Antibody
Functional Invalidation of Putative Sudden Infant Death Syndrome–Associated Variants in the KCNH2-Encoded Kv11.1 Channel | Circulation: Arrhythmia and Electrophysiology
