Frontiers | Electrophysiological Characteristics of the LQT2 Syndrome Mutation KCNH2-G572S and Regulation by Accessory Protein KCNE2
Biomolecules | Free Full-Text | Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 KCNH2 (hERG) Mutations and Identifying New Patients
Heterozygous KCNH2 variant phenotyping using Flp-In HEK293 and high-throughput automated patch clamp electrophysiology | bioRxiv
Large-scale mutational analysis of Kv11.1 reveals molecular insights into type 2 long QT syndrome | Nature Communications
Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing | Revista Española de Cardiología
Biomolecules | Free Full-Text | Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 KCNH2 (hERG) Mutations and Identifying New Patients
KCNH2 Paralogue Annotation
KCNH2 - Creative Bioarray
Modeling long QT syndrome type 2 on-a-chip via in-depth assessment of isogenic gene-edited 3D cardiac tissues | Science Advances
Functional Invalidation of Putative Sudden Infant Death Syndrome–Associated Variants in the KCNH2-Encoded Kv11.1 Channel | Circulation: Arrhythmia and Electrophysiology
Novel mutation in the KCNH2 gene associated with long QT syndrome | Revista Portuguesa de Cardiologia (English edition)
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 Gene - GeneCards | KCNH2 Protein | KCNH2 Antibody
Cellular properties of C-terminal KCNH2 long QT syndrome mutations: description and divergence from clinical phenotypes. | Semantic Scholar
MSTPublications: June 2020 | Medical Scientist Training Program | Vanderbilt University
Genetic analysis identified a heterozygous KCNH2 mutation. (A) Family... | Download Scientific Diagram
Prolonged QT interval on ECG caused by hERG channel dysfunction.... | Download Scientific Diagram
Molecular pathogenesis of long QT syndrome type 2 - ScienceDirect
Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare KCNH2 Variants | Circulation: Genomic and Precision Medicine
Molecular pathogenesis of long QT syndrome type 2 - ScienceDirect
A Novel Mutation (T65P) in the PAS Domain of the Human Potassium Channel HERG Results in the Long QT Syndrome by Trafficking Deficiency - ScienceDirect
Suppression and Replacement Gene Therapy for KCNH2-Mediated Arrhythmias | Circulation: Genomic and Precision Medicine
Cardiac channelopathies: it's in the genes | Nature Medicine
