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
KCNH2-HERG channel subunit. Localization of the described mutations. | Download Scientific Diagram
A Novel Mutation (T65P) in the PAS Domain of the Human Potassium Channel HERG Results in the Long QT Syndrome by Trafficking Deficiency - ScienceDirect
Tbx20 controls the expression of the KCNH2 gene and of hERG channels | PNAS
KCNH2 Gene - GeneCards | KCNH2 Protein | KCNH2 Antibody
Genetic analysis identified a heterozygous KCNH2 mutation. (A) Family... | Download Scientific Diagram
Suppression and Replacement Gene Therapy for KCNH2-Mediated Arrhythmias | Circulation: Genomic and Precision Medicine
Heterozygous KCNH2 variant phenotyping using Flp-In HEK293 and high-throughput automated patch clamp electrophysiology | bioRxiv
Integrated analysis of the voltage-gated potassium channel-associated gene KCNH2 across cancers | BMC Bioinformatics | Full Text
KCNH2 Gene - GeneCards | KCNH2 Protein | KCNH2 Antibody
Isogenic human pluripotent stem cell pairs reveal the role of a KCNH2 mutation in long‐QT syndrome | The EMBO Journal
Overexpression KCNH2-3.1 potassium channel is associated with neuronal... | Download Scientific Diagram
Novel mutation in the KCNH2 gene associated with long QT syndrome | Revista Portuguesa de Cardiologia (English edition)
KCNH2 - Creative Bioarray
Molecular pathogenesis of long QT syndrome type 2 - ScienceDirect
Isogenic Sets of hiPSC-CMs Harboring Distinct KCNH2 Mutations Differ Functionally and in Susceptibility to Drug-Induced Arrhythmias - ScienceDirect
Long QT Syndrome KCNH2 Variant Induces hERG1a/1b Subunit Imbalance in Patient-Specific Induced Pluripotent Stem Cell–Derived Cardiomyocytes | Circulation: Arrhythmia and Electrophysiology
Prolonged QT interval on ECG caused by hERG channel dysfunction.... | Download Scientific Diagram
Chromatogram of 453delC mutation in the KCNH2 gene (A) and schematic... | Download Scientific Diagram
A novel KCNH2 frameshift mutation (c.46delG) associated with high risk of sudden death in a family with congenital long QT syndrome type 2 | International Journal of Arrhythmia | Full Text
KCNH2 Paralogue Annotation
Synonymous nucleotide modification of the KCNH2 gene affects both mRNA characteristics and translation of the encoded hERG ion channel - Journal of Biological Chemistry
MSTPublications: June 2020 | Medical Scientist Training Program | Vanderbilt University
Frontiers | Electrophysiological Characteristics of the LQT2 Syndrome Mutation KCNH2-G572S and Regulation by Accessory Protein KCNE2
Common Genetic Variation in KCNH2 Is Associated With QT Interval Duration | Circulation
