Novel mutation in the KCNH2 gene associated with long QT syndrome | Revista Portuguesa de Cardiologia (English edition)
MSTPublications: June 2020 | Medical Scientist Training Program | Vanderbilt University
KCNH2 Paralogue Annotation
Cardiac channelopathies: it's in the genes | Nature Medicine
Isogenic Sets of hiPSC-CMs Harboring Distinct KCNH2 Mutations Differ Functionally and in Susceptibility to Drug-Induced Arrhythmias - ScienceDirect
Frontiers | The Linkage Phase of the Polymorphism KCNH2-K897T Influences the Electrophysiological Phenotype in hiPSC Models of LQT2
Molecular pathogenesis of long QT syndrome type 2 - ScienceDirect
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
The novel frameshift mutation. Sequencing analysis of KCNH2 gene in the... | Download Scientific Diagram
Genetic analysis identified a heterozygous KCNH2 mutation. (A) Family... | Download Scientific Diagram
KCNH2-HERG channel subunit. Localization of the described mutations. | Download Scientific Diagram
Suppression and Replacement Gene Therapy for KCNH2-Mediated Arrhythmias | Circulation: Genomic and Precision Medicine
Functional Invalidation of Putative Sudden Infant Death Syndrome–Associated Variants in the KCNH2-Encoded Kv11.1 Channel | Circulation: Arrhythmia and Electrophysiology
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
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
A Novel Mutation (T65P) in the PAS Domain of the Human Potassium Channel HERG Results in the Long QT Syndrome by Trafficking Deficiency - ScienceDirect
IJMS | Free Full-Text | H1153Y-KCNH2 Mutation Identified in a Sudden Arrhythmic Death Syndrome Case Alters Channel Gating
Common Genetic Variation in KCNH2 Is Associated With QT Interval Duration | Circulation
Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing | Revista Española de Cardiología
Heterozygous KCNH2 variant phenotyping using Flp-In HEK293 and high-throughput automated patch clamp electrophysiology | bioRxiv
KCNH2 Gene - GeneCards | KCNH2 Protein | KCNH2 Antibody
Synonymous nucleotide modification of the KCNH2 gene affects both mRNA characteristics and translation of the encoded hERG ion channel - Journal of Biological Chemistry
Chromatogram of 453delC mutation in the KCNH2 gene (A) and schematic... | Download Scientific Diagram
