Phenotypic Spectrum in a Family Sharing a Heterozygous KCNQ3 Variant - Kristen Arredondo, Cortlandt Myers, Emily Hansen-Kiss, Mariam T. Mathew, Vijayakumar Jayaraman, Amy Siemon, Dennis Bartholomew, Gail E. Herman, Mari Mori, 2022
Brain Sciences | Free Full-Text | Neonatal Seizures: An Overview of Genetic Causes and Treatment Options
KCNQ3 (potassium voltage-gated channel subfamily Q member 3) | Gene Report | BioGPS
A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions - ScienceDirect
Invitrogen KCNQ3 Polyclonal Antibody, Invitrogen™ 100 μg; Unconjugated Primary Antibodies K | Fisher Scientific
KCNQ2 gene
Protein structure - KCNQ3 - The Human Protein Atlas
Location of 29 mutations in the KCNQ2 gene and three mutations in the... | Download Scientific Diagram
Enigmatic encephalopathies | μNEURO | University of Antwerp
KCNQ2 and KCNQ3 Potassium Channel Subunits: Molecular Correlates of the M-Channel | Science
Proposed structure of the voltage-gated K channels KCNQ2 and KCNQ3... | Download Scientific Diagram
KCNQ3 is the principal target of retigabine in CA1 and subicular excitatory neurons | Journal of Neurophysiology
Gene: KCNQ3 (ENSG00000184156) - Summary - Homo_sapiens - Ensembl genome browser 109
Human KCNQ3 cDNA ORF Clone, untagged, HG18537-UT | Sino Biological
KvLQT3 - Wikipedia
Kcnq3-Related Disorders disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Neuronal KCNQ potassium channels:physislogy and role in disease | Nature Reviews Neuroscience
![PDF] KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/f830358b21cb24998a6bfe0e7090a660c4b1bc81/4-Figure1-1.png "PDF] KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum. | Semantic Scholar")
PDF] KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum. | Semantic Scholar
Functional consequences of the R227Q and R230C/S/H variants in KCNQ3.... | Download Scientific Diagram
John Libbey Eurotext - Epileptic Disorders - Benign familial infantile epilepsy associated with KCNQ3 mutation: a rare occurrence or an underestimated event?
KCNQ2- and KCNQ3-Associated Epilepsy
